| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.91723755_91723757dup | CA5120319 | ROR2 | c.2748_2750dup (p.Glu917_Gly918insGlu) c.1920+408_1920+410dup (n.1920+408_1920+410dup) n.3216_3218dup c.2328_2330dup (p.Glu777_Gly778insGlu) c.1545_1547dup (p.Glu516_Gly517insGlu) c.2739_2741dup (p.Glu914_Gly915insGlu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723755_91723757del | CA5120318 | ROR2 | c.2748_2750del (p.Glu917del) c.1920+408_1920+410del (n.1920+408_1920+410del) n.3216_3218del c.2328_2330del (p.Glu777del) c.1545_1547del (p.Glu516del) c.2739_2741del (p.Glu914del) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 9 | g.91723755_91723758delinsCTCT | CA1863921513 | ROR2 | c.2736_2739delinsAGAG (p.Ala912=) c.1920+396_1920+399delinsAGAG (n.1920+396_1920+399delinsAGAG) n.3204_3207delinsAGAG c.2316_2319delinsAGAG (p.Ala772=) c.1533_1536delinsAGAG (p.Ala511=) c.2727_2730delinsAGAG (p.Ala909=) | |
| 9 | g.91723756T>A | CA373793184 | ROR2 | c.2738A>T (p.Glu913Val) c.1920+398A>T (n.1920+398A>T) n.3206A>T c.2318A>T (p.Glu773Val) c.1535A>T (p.Glu512Val) c.2729A>T (p.Glu910Val) | |
| 9 | g.91723756T>C | CA373793186 | ROR2 | c.2738A>G (p.Glu913Gly) c.1920+398A>G (n.1920+398A>G) n.3206A>G c.2318A>G (p.Glu773Gly) c.1535A>G (p.Glu512Gly) c.2729A>G (p.Glu910Gly) | gnomAD v4 |
| 9 | g.91723756T>G | CA373793185 | ROR2 | c.2738A>C (p.Glu913Ala) c.1920+398A>C (n.1920+398A>C) n.3206A>C c.2318A>C (p.Glu773Ala) c.1535A>C (p.Glu512Ala) c.2729A>C (p.Glu910Ala) | dbSNP gnomAD v2 |
| 9 | g.91723756T= | CA1863921516 | ROR2 | c.2738A= (p.Glu913=) c.1920+398A= (n.1920+398A=) n.3206A= c.2318A= (p.Glu773=) c.1535A= (p.Glu512=) c.2729A= (p.Glu910=) | |
| 9 | g.91723756_91723758del | CA5120321 | ROR2 | c.2736_2738del (p.Glu913del) c.1920+396_1920+398del (n.1920+396_1920+398del) n.3204_3206del c.2316_2318del (p.Glu773del) c.1533_1535del (p.Glu512del) c.2727_2729del (p.Glu910del) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723757C>A | CA373793187 | ROR2 | c.2737G>T (p.Glu913Ter) c.1920+397G>T (n.1920+397G>T) n.3205G>T c.2317G>T (p.Glu773Ter) c.1534G>T (p.Glu512Ter) c.2728G>T (p.Glu910Ter) | |
| 9 | g.91723757C= | CA1863921520 | ROR2 | c.2737G= (p.Glu913=) c.1920+397G= (n.1920+397G=) n.3205G= c.2317G= (p.Glu773=) c.1534G= (p.Glu512=) c.2728G= (p.Glu910=) | |
| 9 | g.91723757C>G | CA373793188 | ROR2 | c.2737G>C (p.Glu913Gln) c.1920+397G>C (n.1920+397G>C) n.3205G>C c.2317G>C (p.Glu773Gln) c.1534G>C (p.Glu512Gln) c.2728G>C (p.Glu910Gln) | dbSNP |
| 9 | g.91723757C>T | CA373793189 | ROR2 | c.2737G>A (p.Glu913Lys) c.1920+397G>A (n.1920+397G>A) n.3205G>A c.2317G>A (p.Glu773Lys) c.1534G>A (p.Glu512Lys) c.2728G>A (p.Glu910Lys) | |
| 9 | g.91723758T>A | CA465995507 | ROR2 | c.2736A>T (p.Ala912=) c.1920+396A>T (n.1920+396A>T) n.3204A>T c.2316A>T (p.Ala772=) c.1533A>T (p.Ala511=) c.2727A>T (p.Ala909=) | |
| 9 | g.91723758T>C | CA465995508 | ROR2 | c.2736A>G (p.Ala912=) c.1920+396A>G (n.1920+396A>G) n.3204A>G c.2316A>G (p.Ala772=) c.1533A>G (p.Ala511=) c.2727A>G (p.Ala909=) | |
| 9 | g.91723758T>G | CA465995510 | ROR2 | c.2736A>C (p.Ala912=) c.1920+396A>C (n.1920+396A>C) n.3204A>C c.2316A>C (p.Ala772=) c.1533A>C (p.Ala511=) c.2727A>C (p.Ala909=) | |
| 9 | g.91723759G>A | CA373793190 | ROR2 | c.2735C>T (p.Ala912Val) c.1920+395C>T (n.1920+395C>T) n.3203C>T c.2315C>T (p.Ala772Val) c.1532C>T (p.Ala511Val) c.2726C>T (p.Ala909Val) | |
| 9 | g.91723759G>C | CA373793191 | ROR2 | c.2735C>G (p.Ala912Gly) c.1920+395C>G (n.1920+395C>G) n.3203C>G c.2315C>G (p.Ala772Gly) c.1532C>G (p.Ala511Gly) c.2726C>G (p.Ala909Gly) | |
| 9 | g.91723759G>T | CA373793192 | ROR2 | c.2735C>A (p.Ala912Glu) c.1920+395C>A (n.1920+395C>A) n.3203C>A c.2315C>A (p.Ala772Glu) c.1532C>A (p.Ala511Glu) c.2726C>A (p.Ala909Glu) | gnomAD v4 |
| 9 | g.91723760C>A | CA373793193 | ROR2 | c.2734G>T (p.Ala912Ser) c.1920+394G>T (n.1920+394G>T) n.3202G>T c.2314G>T (p.Ala772Ser) c.1531G>T (p.Ala511Ser) c.2725G>T (p.Ala909Ser) | |
| 9 | g.91723760C= | CA1863921522 | ROR2 | c.2734G= (p.Ala912=) c.1920+394G= (n.1920+394G=) n.3202G= c.2314G= (p.Ala772=) c.1531G= (p.Ala511=) c.2725G= (p.Ala909=) | |
| 9 | g.91723760C>G | CA373793194 | ROR2 | c.2734G>C (p.Ala912Pro) c.1920+394G>C (n.1920+394G>C) n.3202G>C c.2314G>C (p.Ala772Pro) c.1531G>C (p.Ala511Pro) c.2725G>C (p.Ala909Pro) | |
| 9 | g.91723760C>T | CA373793195 | ROR2 | c.2734G>A (p.Ala912Thr) c.1920+394G>A (n.1920+394G>A) n.3202G>A c.2314G>A (p.Ala772Thr) c.1531G>A (p.Ala511Thr) c.2725G>A (p.Ala909Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723761T>A | CA373793197 | ROR2 | c.2733A>T (p.Glu911Asp) c.1920+393A>T (n.1920+393A>T) n.3201A>T c.2313A>T (p.Glu771Asp) c.1530A>T (p.Glu510Asp) c.2724A>T (p.Glu908Asp) | |
| 9 | g.91723761T>C | CA466334432 | ROR2 | c.2733A>G (p.Glu911=) c.1920+393A>G (n.1920+393A>G) n.3201A>G c.2313A>G (p.Glu771=) c.1530A>G (p.Glu510=) c.2724A>G (p.Glu908=) | |
| 9 | g.91723761T>G | CA373793196 | ROR2 | c.2733A>C (p.Glu911Asp) c.1920+393A>C (n.1920+393A>C) n.3201A>C c.2313A>C (p.Glu771Asp) c.1530A>C (p.Glu510Asp) c.2724A>C (p.Glu908Asp) | |
| 9 | g.91723762T>A | CA373793198 | ROR2 | c.2732A>T (p.Glu911Val) c.1920+392A>T (n.1920+392A>T) n.3200A>T c.2312A>T (p.Glu771Val) c.1529A>T (p.Glu510Val) c.2723A>T (p.Glu908Val) | |
| 9 | g.91723762T>C | CA373793199 | ROR2 | c.2732A>G (p.Glu911Gly) c.1920+392A>G (n.1920+392A>G) n.3200A>G c.2312A>G (p.Glu771Gly) c.1529A>G (p.Glu510Gly) c.2723A>G (p.Glu908Gly) | gnomAD v4 |
| 9 | g.91723762T>G | CA373793200 | ROR2 | c.2732A>C (p.Glu911Ala) c.1920+392A>C (n.1920+392A>C) n.3200A>C c.2312A>C (p.Glu771Ala) c.1529A>C (p.Glu510Ala) c.2723A>C (p.Glu908Ala) | |
| 9 | g.91723763C>A | CA373793201 | ROR2 | c.2731G>T (p.Glu911Ter) c.1920+391G>T (n.1920+391G>T) n.3199G>T c.2311G>T (p.Glu771Ter) c.1528G>T (p.Glu510Ter) c.2722G>T (p.Glu908Ter) | gnomAD v4 |
| 9 | g.91723763C= | CA1863921527 | ROR2 | c.2731G= (p.Glu911=) c.1920+391G= (n.1920+391G=) n.3199G= c.2311G= (p.Glu771=) c.1528G= (p.Glu510=) c.2722G= (p.Glu908=) | |
| 9 | g.91723763C>G | CA373793202 | ROR2 | c.2731G>C (p.Glu911Gln) c.1920+391G>C (n.1920+391G>C) n.3199G>C c.2311G>C (p.Glu771Gln) c.1528G>C (p.Glu510Gln) c.2722G>C (p.Glu908Gln) | |
| 9 | g.91723763C>T | CA373793203 | ROR2 | c.2731G>A (p.Glu911Lys) c.1920+391G>A (n.1920+391G>A) n.3199G>A c.2311G>A (p.Glu771Lys) c.1528G>A (p.Glu510Lys) c.2722G>A (p.Glu908Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723764C>A | CA373793204 | ROR2 | c.2730G>T (p.Gln910His) c.1920+390G>T (n.1920+390G>T) n.3198G>T c.2310G>T (p.Gln770His) c.1527G>T (p.Gln509His) c.2721G>T (p.Gln907His) | |
| 9 | g.91723764C>G | CA373793205 | ROR2 | c.2730G>C (p.Gln910His) c.1920+390G>C (n.1920+390G>C) n.3198G>C c.2310G>C (p.Gln770His) c.1527G>C (p.Gln509His) c.2721G>C (p.Gln907His) | |
| 9 | g.91723764C>T | CA466334433 | ROR2 | c.2730G>A (p.Gln910=) c.1920+390G>A (n.1920+390G>A) n.3198G>A c.2310G>A (p.Gln770=) c.1527G>A (p.Gln509=) c.2721G>A (p.Gln907=) | |
| 9 | g.91723765T>A | CA373793206 | ROR2 | c.2729A>T (p.Gln910Leu) c.1920+389A>T (n.1920+389A>T) n.3197A>T c.2309A>T (p.Gln770Leu) c.1526A>T (p.Gln509Leu) c.2720A>T (p.Gln907Leu) | |
| 9 | g.91723765T>C | CA373793208 | ROR2 | c.2729A>G (p.Gln910Arg) c.1920+389A>G (n.1920+389A>G) n.3197A>G c.2309A>G (p.Gln770Arg) c.1526A>G (p.Gln509Arg) c.2720A>G (p.Gln907Arg) | ClinVar gnomAD v4 |
| 9 | g.91723765T>G | CA373793207 | ROR2 | c.2729A>C (p.Gln910Pro) c.1920+389A>C (n.1920+389A>C) n.3197A>C c.2309A>C (p.Gln770Pro) c.1526A>C (p.Gln509Pro) c.2720A>C (p.Gln907Pro) | |
| 9 | g.91723766G>A | CA373793209 | ROR2 | c.2728C>T (p.Gln910Ter) c.1920+388C>T (n.1920+388C>T) n.3196C>T c.2308C>T (p.Gln770Ter) c.1525C>T (p.Gln509Ter) c.2719C>T (p.Gln907Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723766G>C | CA373793210 | ROR2 | c.2728C>G (p.Gln910Glu) c.1920+388C>G (n.1920+388C>G) n.3196C>G c.2308C>G (p.Gln770Glu) c.1525C>G (p.Gln509Glu) c.2719C>G (p.Gln907Glu) | |
| 9 | g.91723766G= | CA1863921530 | ROR2 | c.2728C= (p.Gln910=) c.1920+388C= (n.1920+388C=) n.3196C= c.2308C= (p.Gln770=) c.1525C= (p.Gln509=) c.2719C= (p.Gln907=) | |
| 9 | g.91723766G>T | CA373793211 | ROR2 | c.2728C>A (p.Gln910Lys) c.1920+388C>A (n.1920+388C>A) n.3196C>A c.2308C>A (p.Gln770Lys) c.1525C>A (p.Gln509Lys) c.2719C>A (p.Gln907Lys) | |
| 9 | g.91723767C>A | CA466334434 | ROR2 | c.2727G>T (p.Val909=) c.1920+387G>T (n.1920+387G>T) n.3195G>T c.2307G>T (p.Val769=) c.1524G>T (p.Val508=) c.2718G>T (p.Val906=) | dbSNP gnomAD v2 |
| 9 | g.91723767C= | CA1863921535 | ROR2 | c.2727G= (p.Val909=) c.1920+387G= (n.1920+387G=) n.3195G= c.2307G= (p.Val769=) c.1524G= (p.Val508=) c.2718G= (p.Val906=) | |
| 9 | g.91723767C>G | CA466334435 | ROR2 | c.2727G>C (p.Val909=) c.1920+387G>C (n.1920+387G>C) n.3195G>C c.2307G>C (p.Val769=) c.1524G>C (p.Val508=) c.2718G>C (p.Val906=) | |
| 9 | g.91723767C>T | CA5120322 | ROR2 | c.2727G>A (p.Val909=) c.1920+387G>A (n.1920+387G>A) n.3195G>A c.2307G>A (p.Val769=) c.1524G>A (p.Val508=) c.2718G>A (p.Val906=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723768A= | CA1863921539 | ROR2 | c.2726T= (p.Val909=) c.1920+386T= (n.1920+386T=) n.3194T= c.2306T= (p.Val769=) c.1523T= (p.Val508=) c.2717T= (p.Val906=) | |
| 9 | g.91723768A>C | CA373793212 | ROR2 | c.2726T>G (p.Val909Gly) c.1920+386T>G (n.1920+386T>G) n.3194T>G c.2306T>G (p.Val769Gly) c.1523T>G (p.Val508Gly) c.2717T>G (p.Val906Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91723768A>G | CA373793214 | ROR2 | c.2726T>C (p.Val909Ala) c.1920+386T>C (n.1920+386T>C) n.3194T>C c.2306T>C (p.Val769Ala) c.1523T>C (p.Val508Ala) c.2717T>C (p.Val906Ala) | |
| 9 | g.91723768A>T | CA373793213 | ROR2 | c.2726T>A (p.Val909Glu) c.1920+386T>A (n.1920+386T>A) n.3194T>A c.2306T>A (p.Val769Glu) c.1523T>A (p.Val508Glu) c.2717T>A (p.Val906Glu) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723769C>A | CA373793215 | ROR2 | c.2725G>T (p.Val909Leu) c.1920+385G>T (n.1920+385G>T) n.3193G>T c.2305G>T (p.Val769Leu) c.1522G>T (p.Val508Leu) c.2716G>T (p.Val906Leu) | |
| 9 | g.91723769C= | CA1863921545 | ROR2 | c.2725G= (p.Val909=) c.1920+385G= (n.1920+385G=) n.3193G= c.2305G= (p.Val769=) c.1522G= (p.Val508=) c.2716G= (p.Val906=) | |
| 9 | g.91723769C>G | CA373793216 | ROR2 | c.2725G>C (p.Val909Leu) c.1920+385G>C (n.1920+385G>C) n.3193G>C c.2305G>C (p.Val769Leu) c.1522G>C (p.Val508Leu) c.2716G>C (p.Val906Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723769C>T | CA5120323 | ROR2 | c.2725G>A (p.Val909Met) c.1920+385G>A (n.1920+385G>A) n.3193G>A c.2305G>A (p.Val769Met) c.1522G>A (p.Val508Met) c.2716G>A (p.Val906Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 9 | g.91723770G>A | CA5120324 | ROR2 | c.2724C>T (p.Thr908=) c.1920+384C>T (n.1920+384C>T) n.3192C>T c.2304C>T (p.Thr768=) c.1521C>T (p.Thr507=) c.2715C>T (p.Thr905=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723770G>C | CA466334436 | ROR2 | c.2724C>G (p.Thr908=) c.1920+384C>G (n.1920+384C>G) n.3192C>G c.2304C>G (p.Thr768=) c.1521C>G (p.Thr507=) c.2715C>G (p.Thr905=) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723770G= | CA1863921552 | ROR2 | c.2724C= (p.Thr908=) c.1920+384C= (n.1920+384C=) n.3192C= c.2304C= (p.Thr768=) c.1521C= (p.Thr507=) c.2715C= (p.Thr905=) | |
| 9 | g.91723770G>T | CA466334437 | ROR2 | c.2724C>A (p.Thr908=) c.1920+384C>A (n.1920+384C>A) n.3192C>A c.2304C>A (p.Thr768=) c.1521C>A (p.Thr507=) c.2715C>A (p.Thr905=) | COSMIC |
| 9 | g.91723771G>A | CA373793217 | ROR2 | c.2723C>T (p.Thr908Ile) c.1920+383C>T (n.1920+383C>T) n.3191C>T c.2303C>T (p.Thr768Ile) c.1520C>T (p.Thr507Ile) c.2714C>T (p.Thr905Ile) | gnomAD v4 |
| 9 | g.91723771G>C | CA373793218 | ROR2 | c.2723C>G (p.Thr908Ser) c.1920+383C>G (n.1920+383C>G) n.3191C>G c.2303C>G (p.Thr768Ser) c.1520C>G (p.Thr507Ser) c.2714C>G (p.Thr905Ser) | |
| 9 | g.91723771G>T | CA373793219 | ROR2 | c.2723C>A (p.Thr908Asn) c.1920+383C>A (n.1920+383C>A) n.3191C>A c.2303C>A (p.Thr768Asn) c.1520C>A (p.Thr507Asn) c.2714C>A (p.Thr905Asn) | |
| 9 | g.91723772T>A | CA373793220 | ROR2 | c.2722A>T (p.Thr908Ser) c.1920+382A>T (n.1920+382A>T) n.3190A>T c.2302A>T (p.Thr768Ser) c.1519A>T (p.Thr507Ser) c.2713A>T (p.Thr905Ser) | |
| 9 | g.91723772T>C | CA373793221 | ROR2 | c.2722A>G (p.Thr908Ala) c.1920+382A>G (n.1920+382A>G) n.3190A>G c.2302A>G (p.Thr768Ala) c.1519A>G (p.Thr507Ala) c.2713A>G (p.Thr905Ala) | |
| 9 | g.91723772T>G | CA373793222 | ROR2 | c.2722A>C (p.Thr908Pro) c.1920+382A>C (n.1920+382A>C) n.3190A>C c.2302A>C (p.Thr768Pro) c.1519A>C (p.Thr507Pro) c.2713A>C (p.Thr905Pro) | dbSNP |
| 9 | g.91723773G>A | CA195321461 | ROR2 | c.2721C>T (p.Ser907=) c.1920+381C>T (n.1920+381C>T) n.3189C>T c.2301C>T (p.Ser767=) c.1518C>T (p.Ser506=) c.2712C>T (p.Ser904=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723773G>C | CA373793223 | ROR2 | c.2721C>G (p.Ser907Arg) c.1920+381C>G (n.1920+381C>G) n.3189C>G c.2301C>G (p.Ser767Arg) c.1518C>G (p.Ser506Arg) c.2712C>G (p.Ser904Arg) | |
| 9 | g.91723773G= | CA1863921555 | ROR2 | c.2721C= (p.Ser907=) c.1920+381C= (n.1920+381C=) n.3189C= c.2301C= (p.Ser767=) c.1518C= (p.Ser506=) c.2712C= (p.Ser904=) | |
| 9 | g.91723773G>T | CA373793224 | ROR2 | c.2721C>A (p.Ser907Arg) c.1920+381C>A (n.1920+381C>A) n.3189C>A c.2301C>A (p.Ser767Arg) c.1518C>A (p.Ser506Arg) c.2712C>A (p.Ser904Arg) | |
| 9 | g.91723774C>A | CA373793227 | ROR2 | c.2720G>T (p.Ser907Ile) c.1920+380G>T (n.1920+380G>T) n.3188G>T c.2300G>T (p.Ser767Ile) c.1517G>T (p.Ser506Ile) c.2711G>T (p.Ser904Ile) | |
| 9 | g.91723774C>G | CA373793226 | ROR2 | c.2720G>C (p.Ser907Thr) c.1920+380G>C (n.1920+380G>C) n.3188G>C c.2300G>C (p.Ser767Thr) c.1517G>C (p.Ser506Thr) c.2711G>C (p.Ser904Thr) | |
| 9 | g.91723774C>T | CA373793225 | ROR2 | c.2720G>A (p.Ser907Asn) c.1920+380G>A (n.1920+380G>A) n.3188G>A c.2300G>A (p.Ser767Asn) c.1517G>A (p.Ser506Asn) c.2711G>A (p.Ser904Asn) | |
| 9 | g.91723775T>A | CA373793229 | ROR2 | c.2719A>T (p.Ser907Cys) c.1920+379A>T (n.1920+379A>T) n.3187A>T c.2299A>T (p.Ser767Cys) c.1516A>T (p.Ser506Cys) c.2710A>T (p.Ser904Cys) | |
| 9 | g.91723775T>C | CA373793228 | ROR2 | c.2719A>G (p.Ser907Gly) c.1920+379A>G (n.1920+379A>G) n.3187A>G c.2299A>G (p.Ser767Gly) c.1516A>G (p.Ser506Gly) c.2710A>G (p.Ser904Gly) | gnomAD v4 |
| 9 | g.91723775T>G | CA373793230 | ROR2 | c.2719A>C (p.Ser907Arg) c.1920+379A>C (n.1920+379A>C) n.3187A>C c.2299A>C (p.Ser767Arg) c.1516A>C (p.Ser506Arg) c.2710A>C (p.Ser904Arg) | |
| 9 | g.91723776C>A | CA373793231 | ROR2 | c.2718G>T (p.Gln906His) c.1920+378G>T (n.1920+378G>T) n.3186G>T c.2298G>T (p.Gln766His) c.1515G>T (p.Gln505His) c.2709G>T (p.Gln903His) | |
| 9 | g.91723776C>G | CA373793232 | ROR2 | c.2718G>C (p.Gln906His) c.1920+378G>C (n.1920+378G>C) n.3186G>C c.2298G>C (p.Gln766His) c.1515G>C (p.Gln505His) c.2709G>C (p.Gln903His) | |
| 9 | g.91723776C>T | CA466334438 | ROR2 | c.2718G>A (p.Gln906=) c.1920+378G>A (n.1920+378G>A) n.3186G>A c.2298G>A (p.Gln766=) c.1515G>A (p.Gln505=) c.2709G>A (p.Gln903=) | |
| 9 | g.91723777T>A | CA373793233 | ROR2 | c.2717A>T (p.Gln906Leu) c.1920+377A>T (n.1920+377A>T) n.3185A>T c.2297A>T (p.Gln766Leu) c.1514A>T (p.Gln505Leu) c.2708A>T (p.Gln903Leu) | |
| 9 | g.91723777T>C | CA5120325 | ROR2 | c.2717A>G (p.Gln906Arg) c.1920+377A>G (n.1920+377A>G) n.3185A>G c.2297A>G (p.Gln766Arg) c.1514A>G (p.Gln505Arg) c.2708A>G (p.Gln903Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723777T>G | CA373793234 | ROR2 | c.2717A>C (p.Gln906Pro) c.1920+377A>C (n.1920+377A>C) n.3185A>C c.2297A>C (p.Gln766Pro) c.1514A>C (p.Gln505Pro) c.2708A>C (p.Gln903Pro) | |
| 9 | g.91723777T= | CA1863921563 | ROR2 | c.2717A= (p.Gln906=) c.1920+377A= (n.1920+377A=) n.3185A= c.2297A= (p.Gln766=) c.1514A= (p.Gln505=) c.2708A= (p.Gln903=) | |
| 9 | g.91723778G>A | CA373793237 | ROR2 | c.2716C>T (p.Gln906Ter) c.1920+376C>T (n.1920+376C>T) n.3184C>T c.2296C>T (p.Gln766Ter) c.1513C>T (p.Gln505Ter) c.2707C>T (p.Gln903Ter) | gnomAD v4 |
| 9 | g.91723778G>C | CA373793236 | ROR2 | c.2716C>G (p.Gln906Glu) c.1920+376C>G (n.1920+376C>G) n.3184C>G c.2296C>G (p.Gln766Glu) c.1513C>G (p.Gln505Glu) c.2707C>G (p.Gln903Glu) | |
| 9 | g.91723778G>T | CA373793235 | ROR2 | c.2716C>A (p.Gln906Lys) c.1920+376C>A (n.1920+376C>A) n.3184C>A c.2296C>A (p.Gln766Lys) c.1513C>A (p.Gln505Lys) c.2707C>A (p.Gln903Lys) | gnomAD v4 |
| 9 | g.91723779G>A | CA466334439 | ROR2 | c.2715C>T (p.Ala905=) c.1920+375C>T (n.1920+375C>T) n.3183C>T c.2295C>T (p.Ala765=) c.1512C>T (p.Ala504=) c.2706C>T (p.Ala902=) | gnomAD v4 |
| 9 | g.91723779G>C | CA466334440 | ROR2 | c.2715C>G (p.Ala905=) c.1920+375C>G (n.1920+375C>G) n.3183C>G c.2295C>G (p.Ala765=) c.1512C>G (p.Ala504=) c.2706C>G (p.Ala902=) | |
| 9 | g.91723779G>T | CA466334441 | ROR2 | c.2715C>A (p.Ala905=) c.1920+375C>A (n.1920+375C>A) n.3183C>A c.2295C>A (p.Ala765=) c.1512C>A (p.Ala504=) c.2706C>A (p.Ala902=) | |
| 9 | g.91723780G>A | CA373793238 | ROR2 | c.2714C>T (p.Ala905Val) c.1920+374C>T (n.1920+374C>T) n.3182C>T c.2294C>T (p.Ala765Val) c.1511C>T (p.Ala504Val) c.2705C>T (p.Ala902Val) | gnomAD v4 |
| 9 | g.91723780G>C | CA373793239 | ROR2 | c.2714C>G (p.Ala905Gly) c.1920+374C>G (n.1920+374C>G) n.3182C>G c.2294C>G (p.Ala765Gly) c.1511C>G (p.Ala504Gly) c.2705C>G (p.Ala902Gly) | |
| 9 | g.91723780G>T | CA373793240 | ROR2 | c.2714C>A (p.Ala905Asp) c.1920+374C>A (n.1920+374C>A) n.3182C>A c.2294C>A (p.Ala765Asp) c.1511C>A (p.Ala504Asp) c.2705C>A (p.Ala902Asp) | gnomAD v4 |
| 9 | g.91723781C>A | CA373793241 | ROR2 | c.2713G>T (p.Ala905Ser) c.1920+373G>T (n.1920+373G>T) n.3181G>T c.2293G>T (p.Ala765Ser) c.1510G>T (p.Ala504Ser) c.2704G>T (p.Ala902Ser) | |
| 9 | g.91723781C= | CA1863921566 | ROR2 | c.2713G= (p.Ala905=) c.1920+373G= (n.1920+373G=) n.3181G= c.2293G= (p.Ala765=) c.1510G= (p.Ala504=) c.2704G= (p.Ala902=) | |
| 9 | g.91723781C>G | CA5120326 | ROR2 | c.2713G>C (p.Ala905Pro) c.1920+373G>C (n.1920+373G>C) n.3181G>C c.2293G>C (p.Ala765Pro) c.1510G>C (p.Ala504Pro) c.2704G>C (p.Ala902Pro) | ClinVar dbSNP ExAC gnomAD v2 |
| 9 | g.91723781C>T | CA373793242 | ROR2 | c.2713G>A (p.Ala905Thr) c.1920+373G>A (n.1920+373G>A) n.3181G>A c.2293G>A (p.Ala765Thr) c.1510G>A (p.Ala504Thr) c.2704G>A (p.Ala902Thr) | |
| 9 | g.91723782C>A | CA466334442 | ROR2 | c.2712G>T (p.Gly904=) c.1920+372G>T (n.1920+372G>T) n.3180G>T c.2292G>T (p.Gly764=) c.1509G>T (p.Gly503=) c.2703G>T (p.Gly901=) | |
| 9 | g.91723782C>G | CA466334444 | ROR2 | c.2712G>C (p.Gly904=) c.1920+372G>C (n.1920+372G>C) n.3180G>C c.2292G>C (p.Gly764=) c.1509G>C (p.Gly503=) c.2703G>C (p.Gly901=) | |
| 9 | g.91723782C>T | CA466334443 | ROR2 | c.2712G>A (p.Gly904=) c.1920+372G>A (n.1920+372G>A) n.3180G>A c.2292G>A (p.Gly764=) c.1509G>A (p.Gly503=) c.2703G>A (p.Gly901=) | |
| 9 | g.91723783C>A | CA373793244 | ROR2 | c.2711G>T (p.Gly904Val) c.1920+371G>T (n.1920+371G>T) n.3179G>T c.2291G>T (p.Gly764Val) c.1508G>T (p.Gly503Val) c.2702G>T (p.Gly901Val) | |
| 9 | g.91723783C= | CA1863921572 | ROR2 | c.2711G= (p.Gly904=) c.1920+371G= (n.1920+371G=) n.3179G= c.2291G= (p.Gly764=) c.1508G= (p.Gly503=) c.2702G= (p.Gly901=) | |
| 9 | g.91723783C>G | CA373793243 | ROR2 | c.2711G>C (p.Gly904Ala) c.1920+371G>C (n.1920+371G>C) n.3179G>C c.2291G>C (p.Gly764Ala) c.1508G>C (p.Gly503Ala) c.2702G>C (p.Gly901Ala) | |
| 9 | g.91723783C>T | CA5120327 | ROR2 | c.2711G>A (p.Gly904Glu) c.1920+371G>A (n.1920+371G>A) n.3179G>A c.2291G>A (p.Gly764Glu) c.1508G>A (p.Gly503Glu) c.2702G>A (p.Gly901Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723784C>A | CA373793245 | ROR2 | c.2710G>T (p.Gly904Trp) c.1920+370G>T (n.1920+370G>T) n.3178G>T c.2290G>T (p.Gly764Trp) c.1507G>T (p.Gly503Trp) c.2701G>T (p.Gly901Trp) | COSMIC |
| 9 | g.91723784C>G | CA373793246 | ROR2 | c.2710G>C (p.Gly904Arg) c.1920+370G>C (n.1920+370G>C) n.3178G>C c.2290G>C (p.Gly764Arg) c.1507G>C (p.Gly503Arg) c.2701G>C (p.Gly901Arg) | |
| 9 | g.91723784C>T | CA373793247 | ROR2 | c.2710G>A (p.Gly904Arg) c.1920+370G>A (n.1920+370G>A) n.3178G>A c.2290G>A (p.Gly764Arg) c.1507G>A (p.Gly503Arg) c.2701G>A (p.Gly901Arg) | |
| 9 | g.91723785A= | CA1863921575 | ROR2 | c.2709T= (p.Asp903=) c.1920+369T= (n.1920+369T=) n.3177T= c.2289T= (p.Asp763=) c.1506T= (p.Asp502=) c.2700T= (p.Asp900=) | |
| 9 | g.91723785A>C | CA373793248 | ROR2 | c.2709T>G (p.Asp903Glu) c.1920+369T>G (n.1920+369T>G) n.3177T>G c.2289T>G (p.Asp763Glu) c.1506T>G (p.Asp502Glu) c.2700T>G (p.Asp900Glu) | |
| 9 | g.91723785A>G | CA466334445 | ROR2 | c.2709T>C (p.Asp903=) c.1920+369T>C (n.1920+369T>C) n.3177T>C c.2289T>C (p.Asp763=) c.1506T>C (p.Asp502=) c.2700T>C (p.Asp900=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723785A>T | CA373793249 | ROR2 | c.2709T>A (p.Asp903Glu) c.1920+369T>A (n.1920+369T>A) n.3177T>A c.2289T>A (p.Asp763Glu) c.1506T>A (p.Asp502Glu) c.2700T>A (p.Asp900Glu) | |
| 9 | g.91723786T>A | CA373793250 | ROR2 | c.2708A>T (p.Asp903Val) c.1920+368A>T (n.1920+368A>T) n.3176A>T c.2288A>T (p.Asp763Val) c.1505A>T (p.Asp502Val) c.2699A>T (p.Asp900Val) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723786T>C | CA373793251 | ROR2 | c.2708A>G (p.Asp903Gly) c.1920+368A>G (n.1920+368A>G) n.3176A>G c.2288A>G (p.Asp763Gly) c.1505A>G (p.Asp502Gly) c.2699A>G (p.Asp900Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91723786T>G | CA373793252 | ROR2 | c.2708A>C (p.Asp903Ala) c.1920+368A>C (n.1920+368A>C) n.3176A>C c.2288A>C (p.Asp763Ala) c.1505A>C (p.Asp502Ala) c.2699A>C (p.Asp900Ala) | |
| 9 | g.91723786T= | CA1863921581 | ROR2 | c.2708A= (p.Asp903=) c.1920+368A= (n.1920+368A=) n.3176A= c.2288A= (p.Asp763=) c.1505A= (p.Asp502=) c.2699A= (p.Asp900=) | |
| 9 | g.91723787C>A | CA373793253 | ROR2 | c.2707G>T (p.Asp903Tyr) c.1920+367G>T (n.1920+367G>T) n.3175G>T c.2287G>T (p.Asp763Tyr) c.1504G>T (p.Asp502Tyr) c.2698G>T (p.Asp900Tyr) | |
| 9 | g.91723787C= | CA1863921584 | ROR2 | c.2707G= (p.Asp903=) c.1920+367G= (n.1920+367G=) n.3175G= c.2287G= (p.Asp763=) c.1504G= (p.Asp502=) c.2698G= (p.Asp900=) | |
| 9 | g.91723787C>G | CA373793254 | ROR2 | c.2707G>C (p.Asp903His) c.1920+367G>C (n.1920+367G>C) n.3175G>C c.2287G>C (p.Asp763His) c.1504G>C (p.Asp502His) c.2698G>C (p.Asp900His) | |
| 9 | g.91723787C>T | CA373793255 | ROR2 | c.2707G>A (p.Asp903Asn) c.1920+367G>A (n.1920+367G>A) n.3175G>A c.2287G>A (p.Asp763Asn) c.1504G>A (p.Asp502Asn) c.2698G>A (p.Asp900Asn) | dbSNP |
| 9 | g.91723788T>A | CA373793256 | ROR2 | c.2706A>T (p.Glu902Asp) c.1920+366A>T (n.1920+366A>T) n.3174A>T c.2286A>T (p.Glu762Asp) c.1503A>T (p.Glu501Asp) c.2697A>T (p.Glu899Asp) | |
| 9 | g.91723788T>C | CA466334446 | ROR2 | c.2706A>G (p.Glu902=) c.1920+366A>G (n.1920+366A>G) n.3174A>G c.2286A>G (p.Glu762=) c.1503A>G (p.Glu501=) c.2697A>G (p.Glu899=) | |
| 9 | g.91723788T>G | CA373793257 | ROR2 | c.2706A>C (p.Glu902Asp) c.1920+366A>C (n.1920+366A>C) n.3174A>C c.2286A>C (p.Glu762Asp) c.1503A>C (p.Glu501Asp) c.2697A>C (p.Glu899Asp) | |
| 9 | g.91723789T>A | CA373793260 | ROR2 | c.2705A>T (p.Glu902Val) c.1920+365A>T (n.1920+365A>T) n.3173A>T c.2285A>T (p.Glu762Val) c.1502A>T (p.Glu501Val) c.2696A>T (p.Glu899Val) | |
| 9 | g.91723789T>C | CA373793258 | ROR2 | c.2705A>G (p.Glu902Gly) c.1920+365A>G (n.1920+365A>G) n.3173A>G c.2285A>G (p.Glu762Gly) c.1502A>G (p.Glu501Gly) c.2696A>G (p.Glu899Gly) | |
| 9 | g.91723789T>G | CA373793259 | ROR2 | c.2705A>C (p.Glu902Ala) c.1920+365A>C (n.1920+365A>C) n.3173A>C c.2285A>C (p.Glu762Ala) c.1502A>C (p.Glu501Ala) c.2696A>C (p.Glu899Ala) | gnomAD v4 |
| 9 | g.91723790C>A | CA373793261 | ROR2 | c.2704G>T (p.Glu902Ter) c.1920+364G>T (n.1920+364G>T) n.3172G>T c.2284G>T (p.Glu762Ter) c.1501G>T (p.Glu501Ter) c.2695G>T (p.Glu899Ter) | gnomAD v4 |
| 9 | g.91723790C>G | CA373793262 | ROR2 | c.2704G>C (p.Glu902Gln) c.1920+364G>C (n.1920+364G>C) n.3172G>C c.2284G>C (p.Glu762Gln) c.1501G>C (p.Glu501Gln) c.2695G>C (p.Glu899Gln) | |
| 9 | g.91723790C>T | CA373793263 | ROR2 | c.2704G>A (p.Glu902Lys) c.1920+364G>A (n.1920+364G>A) n.3172G>A c.2284G>A (p.Glu762Lys) c.1501G>A (p.Glu501Lys) c.2695G>A (p.Glu899Lys) | |
| 9 | g.91723791T>A | CA466334447 | ROR2 | c.2703A>T (p.Pro901=) c.1920+363A>T (n.1920+363A>T) n.3171A>T c.2283A>T (p.Pro761=) c.1500A>T (p.Pro500=) c.2694A>T (p.Pro898=) | |
| 9 | g.91723791T>C | CA466334448 | ROR2 | c.2703A>G (p.Pro901=) c.1920+363A>G (n.1920+363A>G) n.3171A>G c.2283A>G (p.Pro761=) c.1500A>G (p.Pro500=) c.2694A>G (p.Pro898=) | dbSNP gnomAD v4 |
| 9 | g.91723791T>G | CA466334449 | ROR2 | c.2703A>C (p.Pro901=) c.1920+363A>C (n.1920+363A>C) n.3171A>C c.2283A>C (p.Pro761=) c.1500A>C (p.Pro500=) c.2694A>C (p.Pro898=) | |
| 9 | g.91723791T= | CA1863921586 | ROR2 | c.2703A= (p.Pro901=) c.1920+363A= (n.1920+363A=) n.3171A= c.2283A= (p.Pro761=) c.1500A= (p.Pro500=) c.2694A= (p.Pro898=) | |
| 9 | g.91723792G>A | CA5120328 | ROR2 | c.2702C>T (p.Pro901Leu) c.1920+362C>T (n.1920+362C>T) n.3170C>T c.2282C>T (p.Pro761Leu) c.1499C>T (p.Pro500Leu) c.2693C>T (p.Pro898Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723792G>C | CA373793264 | ROR2 | c.2702C>G (p.Pro901Arg) c.1920+362C>G (n.1920+362C>G) n.3170C>G c.2282C>G (p.Pro761Arg) c.1499C>G (p.Pro500Arg) c.2693C>G (p.Pro898Arg) | |
| 9 | g.91723792G= | CA1863921589 | ROR2 | c.2702C= (p.Pro901=) c.1920+362C= (n.1920+362C=) n.3170C= c.2282C= (p.Pro761=) c.1499C= (p.Pro500=) c.2693C= (p.Pro898=) | |
| 9 | g.91723792G>T | CA373793265 | ROR2 | c.2702C>A (p.Pro901Gln) c.1920+362C>A (n.1920+362C>A) n.3170C>A c.2282C>A (p.Pro761Gln) c.1499C>A (p.Pro500Gln) c.2693C>A (p.Pro898Gln) | gnomAD v4 |
| 9 | g.91723793G>A | CA5120329 | ROR2 | c.2701C>T (p.Pro901Ser) c.1920+361C>T (n.1920+361C>T) n.3169C>T c.2281C>T (p.Pro761Ser) c.1498C>T (p.Pro500Ser) c.2692C>T (p.Pro898Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723793G>C | CA373793267 | ROR2 | c.2701C>G (p.Pro901Ala) c.1920+361C>G (n.1920+361C>G) n.3169C>G c.2281C>G (p.Pro761Ala) c.1498C>G (p.Pro500Ala) c.2692C>G (p.Pro898Ala) | |
| 9 | g.91723793G= | CA1863921594 | ROR2 | c.2701C= (p.Pro901=) c.1920+361C= (n.1920+361C=) n.3169C= c.2281C= (p.Pro761=) c.1498C= (p.Pro500=) c.2692C= (p.Pro898=) | |
| 9 | g.91723793G>T | CA373793266 | ROR2 | c.2701C>A (p.Pro901Thr) c.1920+361C>A (n.1920+361C>A) n.3169C>A c.2281C>A (p.Pro761Thr) c.1498C>A (p.Pro500Thr) c.2692C>A (p.Pro898Thr) | |
| 9 | g.91723794G>A | CA466334450 | ROR2 | c.2700C>T (p.Ala900=) c.1920+360C>T (n.1920+360C>T) n.3168C>T c.2280C>T (p.Ala760=) c.1497C>T (p.Ala499=) c.2691C>T (p.Ala897=) | |
| 9 | g.91723794G>C | CA466334451 | ROR2 | c.2700C>G (p.Ala900=) c.1920+360C>G (n.1920+360C>G) n.3168C>G c.2280C>G (p.Ala760=) c.1497C>G (p.Ala499=) c.2691C>G (p.Ala897=) | |
| 9 | g.91723794G>T | CA466334452 | ROR2 | c.2700C>A (p.Ala900=) c.1920+360C>A (n.1920+360C>A) n.3168C>A c.2280C>A (p.Ala760=) c.1497C>A (p.Ala499=) c.2691C>A (p.Ala897=) | |
| 9 | g.91723795G>A | CA373793268 | ROR2 | c.2699C>T (p.Ala900Val) c.1920+359C>T (n.1920+359C>T) n.3167C>T c.2279C>T (p.Ala760Val) c.1496C>T (p.Ala499Val) c.2690C>T (p.Ala897Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723795G>C | CA373793269 | ROR2 | c.2699C>G (p.Ala900Gly) c.1920+359C>G (n.1920+359C>G) n.3167C>G c.2279C>G (p.Ala760Gly) c.1496C>G (p.Ala499Gly) c.2690C>G (p.Ala897Gly) | |
| 9 | g.91723795G= | CA1863921596 | ROR2 | c.2699C= (p.Ala900=) c.1920+359C= (n.1920+359C=) n.3167C= c.2279C= (p.Ala760=) c.1496C= (p.Ala499=) c.2690C= (p.Ala897=) | |
| 9 | g.91723795G>T | CA373793270 | ROR2 | c.2699C>A (p.Ala900Asp) c.1920+359C>A (n.1920+359C>A) n.3167C>A c.2279C>A (p.Ala760Asp) c.1496C>A (p.Ala499Asp) c.2690C>A (p.Ala897Asp) | gnomAD v4 |
| 9 | g.91723796C>A | CA5120331 | ROR2 | c.2698G>T (p.Ala900Ser) c.1920+358G>T (n.1920+358G>T) n.3166G>T c.2278G>T (p.Ala760Ser) c.1495G>T (p.Ala499Ser) c.2689G>T (p.Ala897Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723796C= | CA1863921598 | ROR2 | c.2698G= (p.Ala900=) c.1920+358G= (n.1920+358G=) n.3166G= c.2278G= (p.Ala760=) c.1495G= (p.Ala499=) c.2689G= (p.Ala897=) | |
| 9 | g.91723796C>G | CA373793271 | ROR2 | c.2698G>C (p.Ala900Pro) c.1920+358G>C (n.1920+358G>C) n.3166G>C c.2278G>C (p.Ala760Pro) c.1495G>C (p.Ala499Pro) c.2689G>C (p.Ala897Pro) | gnomAD v4 |
| 9 | g.91723796C>T | CA5120330 | ROR2 | c.2698G>A (p.Ala900Thr) c.1920+358G>A (n.1920+358G>A) n.3166G>A c.2278G>A (p.Ala760Thr) c.1495G>A (p.Ala499Thr) c.2689G>A (p.Ala897Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91723797G>A | CA5120332 | ROR2 | c.2697C>T (p.Asn899=) c.1920+357C>T (n.1920+357C>T) n.3165C>T c.2277C>T (p.Asn759=) c.1494C>T (p.Asn498=) c.2688C>T (p.Asn896=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723797G>C | CA373793273 | ROR2 | c.2697C>G (p.Asn899Lys) c.1920+357C>G (n.1920+357C>G) n.3165C>G c.2277C>G (p.Asn759Lys) c.1494C>G (p.Asn498Lys) c.2688C>G (p.Asn896Lys) | |
| 9 | g.91723797G= | CA1863921601 | ROR2 | c.2697C= (p.Asn899=) c.1920+357C= (n.1920+357C=) n.3165C= c.2277C= (p.Asn759=) c.1494C= (p.Asn498=) c.2688C= (p.Asn896=) | |
| 9 | g.91723797G>T | CA373793272 | ROR2 | c.2697C>A (p.Asn899Lys) c.1920+357C>A (n.1920+357C>A) n.3165C>A c.2277C>A (p.Asn759Lys) c.1494C>A (p.Asn498Lys) c.2688C>A (p.Asn896Lys) | dbSNP |
| 9 | g.91723798T>A | CA373793274 | ROR2 | c.2696A>T (p.Asn899Ile) c.1920+356A>T (n.1920+356A>T) n.3164A>T c.2276A>T (p.Asn759Ile) c.1493A>T (p.Asn498Ile) c.2687A>T (p.Asn896Ile) | |
| 9 | g.91723798T>C | CA373793275 | ROR2 | c.2696A>G (p.Asn899Ser) c.1920+356A>G (n.1920+356A>G) n.3164A>G c.2276A>G (p.Asn759Ser) c.1493A>G (p.Asn498Ser) c.2687A>G (p.Asn896Ser) | |
| 9 | g.91723798T>G | CA373793276 | ROR2 | c.2696A>C (p.Asn899Thr) c.1920+356A>C (n.1920+356A>C) n.3164A>C c.2276A>C (p.Asn759Thr) c.1493A>C (p.Asn498Thr) c.2687A>C (p.Asn896Thr) | |
| 9 | g.91723799T>A | CA373793277 | ROR2 | c.2695A>T (p.Asn899Tyr) c.1920+355A>T (n.1920+355A>T) n.3163A>T c.2275A>T (p.Asn759Tyr) c.1492A>T (p.Asn498Tyr) c.2686A>T (p.Asn896Tyr) | |
| 9 | g.91723799T>C | CA373793278 | ROR2 | c.2695A>G (p.Asn899Asp) c.1920+355A>G (n.1920+355A>G) n.3163A>G c.2275A>G (p.Asn759Asp) c.1492A>G (p.Asn498Asp) c.2686A>G (p.Asn896Asp) | |
| 9 | g.91723799T>G | CA373793279 | ROR2 | c.2695A>C (p.Asn899His) c.1920+355A>C (n.1920+355A>C) n.3163A>C c.2275A>C (p.Asn759His) c.1492A>C (p.Asn498His) c.2686A>C (p.Asn896His) | |
| 9 | g.91723800C>A | CA373793280 | ROR2 | c.2694G>T (p.Gln898His) c.1920+354G>T (n.1920+354G>T) n.3162G>T c.2274G>T (p.Gln758His) c.1491G>T (p.Gln497His) c.2685G>T (p.Gln895His) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723800C= | CA1863921608 | ROR2 | c.2694G= (p.Gln898=) c.1920+354G= (n.1920+354G=) n.3162G= c.2274G= (p.Gln758=) c.1491G= (p.Gln497=) c.2685G= (p.Gln895=) | |
| 9 | g.91723800C>G | CA5120333 | ROR2 | c.2694G>C (p.Gln898His) c.1920+354G>C (n.1920+354G>C) n.3162G>C c.2274G>C (p.Gln758His) c.1491G>C (p.Gln497His) c.2685G>C (p.Gln895His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723800C>T | CA466334453 | ROR2 | c.2694G>A (p.Gln898=) c.1920+354G>A (n.1920+354G>A) n.3162G>A c.2274G>A (p.Gln758=) c.1491G>A (p.Gln497=) c.2685G>A (p.Gln895=) | gnomAD v4 COSMIC |
| 9 | g.91723801T>A | CA373793281 | ROR2 | c.2693A>T (p.Gln898Leu) c.1920+353A>T (n.1920+353A>T) n.3161A>T c.2273A>T (p.Gln758Leu) c.1490A>T (p.Gln497Leu) c.2684A>T (p.Gln895Leu) | |
| 9 | g.91723801T>C | CA373793282 | ROR2 | c.2693A>G (p.Gln898Arg) c.1920+353A>G (n.1920+353A>G) n.3161A>G c.2273A>G (p.Gln758Arg) c.1490A>G (p.Gln497Arg) c.2684A>G (p.Gln895Arg) | ClinVar gnomAD v4 |
| 9 | g.91723801T>G | CA373793283 | ROR2 | c.2693A>C (p.Gln898Pro) c.1920+353A>C (n.1920+353A>C) n.3161A>C c.2273A>C (p.Gln758Pro) c.1490A>C (p.Gln497Pro) c.2684A>C (p.Gln895Pro) | |
| 9 | g.91723802G>A | CA373793285 | ROR2 | c.2692C>T (p.Gln898Ter) c.1920+352C>T (n.1920+352C>T) n.3160C>T c.2272C>T (p.Gln758Ter) c.1489C>T (p.Gln497Ter) c.2683C>T (p.Gln895Ter) | gnomAD v4 |
| 9 | g.91723802G>C | CA5120334 | ROR2 | c.2692C>G (p.Gln898Glu) c.1920+352C>G (n.1920+352C>G) n.3160C>G c.2272C>G (p.Gln758Glu) c.1489C>G (p.Gln497Glu) c.2683C>G (p.Gln895Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723802G= | CA1863921614 | ROR2 | c.2692C= (p.Gln898=) c.1920+352C= (n.1920+352C=) n.3160C= c.2272C= (p.Gln758=) c.1489C= (p.Gln497=) c.2683C= (p.Gln895=) | |
| 9 | g.91723802G>T | CA373793284 | ROR2 | c.2692C>A (p.Gln898Lys) c.1920+352C>A (n.1920+352C>A) n.3160C>A c.2272C>A (p.Gln758Lys) c.1489C>A (p.Gln497Lys) c.2683C>A (p.Gln895Lys) | |
| 9 | g.91723803T>A | CA466334456 | ROR2 | c.2691A>T (p.Thr897=) c.1920+351A>T (n.1920+351A>T) n.3159A>T c.2271A>T (p.Thr757=) c.1488A>T (p.Thr496=) c.2682A>T (p.Thr894=) | |
| 9 | g.91723803T>C | CA466334454 | ROR2 | c.2691A>G (p.Thr897=) c.1920+351A>G (n.1920+351A>G) n.3159A>G c.2271A>G (p.Thr757=) c.1488A>G (p.Thr496=) c.2682A>G (p.Thr894=) | |
| 9 | g.91723803T>G | CA466334455 | ROR2 | c.2691A>C (p.Thr897=) c.1920+351A>C (n.1920+351A>C) n.3159A>C c.2271A>C (p.Thr757=) c.1488A>C (p.Thr496=) c.2682A>C (p.Thr894=) | |
| 9 | g.91723804G>A | CA373793286 | ROR2 | c.2690C>T (p.Thr897Ile) c.1920+350C>T (n.1920+350C>T) n.3158C>T c.2270C>T (p.Thr757Ile) c.1487C>T (p.Thr496Ile) c.2681C>T (p.Thr894Ile) | |
| 9 | g.91723804G>C | CA373793287 | ROR2 | c.2690C>G (p.Thr897Arg) c.1920+350C>G (n.1920+350C>G) n.3158C>G c.2270C>G (p.Thr757Arg) c.1487C>G (p.Thr496Arg) c.2681C>G (p.Thr894Arg) | |
| 9 | g.91723804G>T | CA373793288 | ROR2 | c.2690C>A (p.Thr897Lys) c.1920+350C>A (n.1920+350C>A) n.3158C>A c.2270C>A (p.Thr757Lys) c.1487C>A (p.Thr496Lys) c.2681C>A (p.Thr894Lys) | gnomAD v4 |
| 9 | g.91723805T>A | CA373793289 | ROR2 | c.2689A>T (p.Thr897Ser) c.1920+349A>T (n.1920+349A>T) n.3157A>T c.2269A>T (p.Thr757Ser) c.1486A>T (p.Thr496Ser) c.2680A>T (p.Thr894Ser) | gnomAD v4 |
| 9 | g.91723805T>C | CA373793290 | ROR2 | c.2689A>G (p.Thr897Ala) c.1920+349A>G (n.1920+349A>G) n.3157A>G c.2269A>G (p.Thr757Ala) c.1486A>G (p.Thr496Ala) c.2680A>G (p.Thr894Ala) | |
| 9 | g.91723805T>G | CA373793291 | ROR2 | c.2689A>C (p.Thr897Pro) c.1920+349A>C (n.1920+349A>C) n.3157A>C c.2269A>C (p.Thr757Pro) c.1486A>C (p.Thr496Pro) c.2680A>C (p.Thr894Pro) | |
| 9 | g.91723806G>A | CA466334457 | ROR2 | c.2688C>T (p.Asp896=) c.1920+348C>T (n.1920+348C>T) n.3156C>T c.2268C>T (p.Asp756=) c.1485C>T (p.Asp495=) c.2679C>T (p.Asp893=) | gnomAD v4 |
| 9 | g.91723806G>C | CA373793292 | ROR2 | c.2688C>G (p.Asp896Glu) c.1920+348C>G (n.1920+348C>G) n.3156C>G c.2268C>G (p.Asp756Glu) c.1485C>G (p.Asp495Glu) c.2679C>G (p.Asp893Glu) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723806G= | CA1863921621 | ROR2 | c.2688C= (p.Asp896=) c.1920+348C= (n.1920+348C=) n.3156C= c.2268C= (p.Asp756=) c.1485C= (p.Asp495=) c.2679C= (p.Asp893=) | |
| 9 | g.91723806G>T | CA373793293 | ROR2 | c.2688C>A (p.Asp896Glu) c.1920+348C>A (n.1920+348C>A) n.3156C>A c.2268C>A (p.Asp756Glu) c.1485C>A (p.Asp495Glu) c.2679C>A (p.Asp893Glu) | |
| 9 | g.91723807T>A | CA373793294 | ROR2 | c.2687A>T (p.Asp896Val) c.1920+347A>T (n.1920+347A>T) n.3155A>T c.2267A>T (p.Asp756Val) c.1484A>T (p.Asp495Val) c.2678A>T (p.Asp893Val) | |
| 9 | g.91723807T>C | CA373793295 | ROR2 | c.2687A>G (p.Asp896Gly) c.1920+347A>G (n.1920+347A>G) n.3155A>G c.2267A>G (p.Asp756Gly) c.1484A>G (p.Asp495Gly) c.2678A>G (p.Asp893Gly) | |
| 9 | g.91723807T>G | CA373793296 | ROR2 | c.2687A>C (p.Asp896Ala) c.1920+347A>C (n.1920+347A>C) n.3155A>C c.2267A>C (p.Asp756Ala) c.1484A>C (p.Asp495Ala) c.2678A>C (p.Asp893Ala) | |
| 9 | g.91723808C>A | CA373793297 | ROR2 | c.2686G>T (p.Asp896Tyr) c.1920+346G>T (n.1920+346G>T) n.3154G>T c.2266G>T (p.Asp756Tyr) c.1483G>T (p.Asp495Tyr) c.2677G>T (p.Asp893Tyr) | |
| 9 | g.91723808C>G | CA373793298 | ROR2 | c.2686G>C (p.Asp896His) c.1920+346G>C (n.1920+346G>C) n.3154G>C c.2266G>C (p.Asp756His) c.1483G>C (p.Asp495His) c.2677G>C (p.Asp893His) | |
| 9 | g.91723808C>T | CA373793299 | ROR2 | c.2686G>A (p.Asp896Asn) c.1920+346G>A (n.1920+346G>A) n.3154G>A c.2266G>A (p.Asp756Asn) c.1483G>A (p.Asp495Asn) c.2677G>A (p.Asp893Asn) | gnomAD v4 |
| 9 | g.91723809A= | CA1863921624 | ROR2 | c.2685T= (p.Asp895=) c.1920+345T= (n.1920+345T=) n.3153T= c.2265T= (p.Asp755=) c.1482T= (p.Asp494=) c.2676T= (p.Asp892=) | |
| 9 | g.91723809A>C | CA373793301 | ROR2 | c.2685T>G (p.Asp895Glu) c.1920+345T>G (n.1920+345T>G) n.3153T>G c.2265T>G (p.Asp755Glu) c.1482T>G (p.Asp494Glu) c.2676T>G (p.Asp892Glu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723809A>G | CA466334458 | ROR2 | c.2685T>C (p.Asp895=) c.1920+345T>C (n.1920+345T>C) n.3153T>C c.2265T>C (p.Asp755=) c.1482T>C (p.Asp494=) c.2676T>C (p.Asp892=) | dbSNP |
| 9 | g.91723809A>T | CA373793300 | ROR2 | c.2685T>A (p.Asp895Glu) c.1920+345T>A (n.1920+345T>A) n.3153T>A c.2265T>A (p.Asp755Glu) c.1482T>A (p.Asp494Glu) c.2676T>A (p.Asp892Glu) | gnomAD v4 |
| 9 | g.91723810T>A | CA373793302 | ROR2 | c.2684A>T (p.Asp895Val) c.1920+344A>T (n.1920+344A>T) n.3152A>T c.2264A>T (p.Asp755Val) c.1481A>T (p.Asp494Val) c.2675A>T (p.Asp892Val) | gnomAD v4 |
| 9 | g.91723810T>C | CA5120335 | ROR2 | c.2684A>G (p.Asp895Gly) c.1920+344A>G (n.1920+344A>G) n.3152A>G c.2264A>G (p.Asp755Gly) c.1481A>G (p.Asp494Gly) c.2675A>G (p.Asp892Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723810T>G | CA373793303 | ROR2 | c.2684A>C (p.Asp895Ala) c.1920+344A>C (n.1920+344A>C) n.3152A>C c.2264A>C (p.Asp755Ala) c.1481A>C (p.Asp494Ala) c.2675A>C (p.Asp892Ala) | |
| 9 | g.91723810T= | CA1863921625 | ROR2 | c.2684A= (p.Asp895=) c.1920+344A= (n.1920+344A=) n.3152A= c.2264A= (p.Asp755=) c.1481A= (p.Asp494=) c.2675A= (p.Asp892=) | |
| 9 | g.91723811C>A | CA373793304 | ROR2 | c.2683G>T (p.Asp895Tyr) c.1920+343G>T (n.1920+343G>T) n.3151G>T c.2263G>T (p.Asp755Tyr) c.1480G>T (p.Asp494Tyr) c.2674G>T (p.Asp892Tyr) | |
| 9 | g.91723811C= | CA1863921627 | ROR2 | c.2683G= (p.Asp895=) c.1920+343G= (n.1920+343G=) n.3151G= c.2263G= (p.Asp755=) c.1480G= (p.Asp494=) c.2674G= (p.Asp892=) | |
| 9 | g.91723811C>G | CA373793305 | ROR2 | c.2683G>C (p.Asp895His) c.1920+343G>C (n.1920+343G>C) n.3151G>C c.2263G>C (p.Asp755His) c.1480G>C (p.Asp494His) c.2674G>C (p.Asp892His) | |
| 9 | g.91723811C>T | CA373793306 | ROR2 | c.2683G>A (p.Asp895Asn) c.1920+343G>A (n.1920+343G>A) n.3151G>A c.2263G>A (p.Asp755Asn) c.1480G>A (p.Asp494Asn) c.2674G>A (p.Asp892Asn) | dbSNP gnomAD v4 |
| 9 | g.91723812A= | CA1863921629 | ROR2 | c.2682T= (p.Ala894=) c.1920+342T= (n.1920+342T=) n.3150T= c.2262T= (p.Ala754=) c.1479T= (p.Ala493=) c.2673T= (p.Ala891=) | |
| 9 | g.91723812A>C | CA5120336 | ROR2 | c.2682T>G (p.Ala894=) c.1920+342T>G (n.1920+342T>G) n.3150T>G c.2262T>G (p.Ala754=) c.1479T>G (p.Ala493=) c.2673T>G (p.Ala891=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723812A>G | CA466334459 | ROR2 | c.2682T>C (p.Ala894=) c.1920+342T>C (n.1920+342T>C) n.3150T>C c.2262T>C (p.Ala754=) c.1479T>C (p.Ala493=) c.2673T>C (p.Ala891=) | dbSNP |
| 9 | g.91723812A>T | CA466334460 | ROR2 | c.2682T>A (p.Ala894=) c.1920+342T>A (n.1920+342T>A) n.3150T>A c.2262T>A (p.Ala754=) c.1479T>A (p.Ala493=) c.2673T>A (p.Ala891=) | |
| 9 | g.91723813G>A | CA373793307 | ROR2 | c.2681C>T (p.Ala894Val) c.1920+341C>T (n.1920+341C>T) n.3149C>T c.2261C>T (p.Ala754Val) c.1478C>T (p.Ala493Val) c.2672C>T (p.Ala891Val) | |
| 9 | g.91723813G>C | CA373793309 | ROR2 | c.2681C>G (p.Ala894Gly) c.1920+341C>G (n.1920+341C>G) n.3149C>G c.2261C>G (p.Ala754Gly) c.1478C>G (p.Ala493Gly) c.2672C>G (p.Ala891Gly) | |
| 9 | g.91723813G>T | CA373793308 | ROR2 | c.2681C>A (p.Ala894Asp) c.1920+341C>A (n.1920+341C>A) n.3149C>A c.2261C>A (p.Ala754Asp) c.1478C>A (p.Ala493Asp) c.2672C>A (p.Ala891Asp) | |
| 9 | g.91723814C>A | CA373793310 | ROR2 | c.2680G>T (p.Ala894Ser) c.1920+340G>T (n.1920+340G>T) n.3148G>T c.2260G>T (p.Ala754Ser) c.1477G>T (p.Ala493Ser) c.2671G>T (p.Ala891Ser) | gnomAD v4 COSMIC |
| 9 | g.91723814C= | CA1863921631 | ROR2 | c.2680G= (p.Ala894=) c.1920+340G= (n.1920+340G=) n.3148G= c.2260G= (p.Ala754=) c.1477G= (p.Ala493=) c.2671G= (p.Ala891=) | |
| 9 | g.91723814C>G | CA373793311 | ROR2 | c.2680G>C (p.Ala894Pro) c.1920+340G>C (n.1920+340G>C) n.3148G>C c.2260G>C (p.Ala754Pro) c.1477G>C (p.Ala493Pro) c.2671G>C (p.Ala891Pro) | |
| 9 | g.91723814C>T | CA373793312 | ROR2 | c.2680G>A (p.Ala894Thr) c.1920+340G>A (n.1920+340G>A) n.3148G>A c.2260G>A (p.Ala754Thr) c.1477G>A (p.Ala493Thr) c.2671G>A (p.Ala891Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91723815G>A | CA5120337 | ROR2 | c.2679C>T (p.Gly893=) c.1920+339C>T (n.1920+339C>T) n.3147C>T c.2259C>T (p.Gly753=) c.1476C>T (p.Gly492=) c.2670C>T (p.Gly890=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723815G>C | CA466334461 | ROR2 | c.2679C>G (p.Gly893=) c.1920+339C>G (n.1920+339C>G) n.3147C>G c.2259C>G (p.Gly753=) c.1476C>G (p.Gly492=) c.2670C>G (p.Gly890=) | |
| 9 | g.91723815G= | CA1863921635 | ROR2 | c.2679C= (p.Gly893=) c.1920+339C= (n.1920+339C=) n.3147C= c.2259C= (p.Gly753=) c.1476C= (p.Gly492=) c.2670C= (p.Gly890=) | |
| 9 | g.91723815G>T | CA466334462 | ROR2 | c.2679C>A (p.Gly893=) c.1920+339C>A (n.1920+339C>A) n.3147C>A c.2259C>A (p.Gly753=) c.1476C>A (p.Gly492=) c.2670C>A (p.Gly890=) | |
| 9 | g.91723816C>A | CA373793315 | ROR2 | c.2678G>T (p.Gly893Val) c.1920+338G>T (n.1920+338G>T) n.3146G>T c.2258G>T (p.Gly753Val) c.1475G>T (p.Gly492Val) c.2669G>T (p.Gly890Val) | |
| 9 | g.91723816C>G | CA373793313 | ROR2 | c.2678G>C (p.Gly893Ala) c.1920+338G>C (n.1920+338G>C) n.3146G>C c.2258G>C (p.Gly753Ala) c.1475G>C (p.Gly492Ala) c.2669G>C (p.Gly890Ala) | |
| 9 | g.91723816C>T | CA373793314 | ROR2 | c.2678G>A (p.Gly893Asp) c.1920+338G>A (n.1920+338G>A) n.3146G>A c.2258G>A (p.Gly753Asp) c.1475G>A (p.Gly492Asp) c.2669G>A (p.Gly890Asp) | gnomAD v4 COSMIC |
| 9 | g.91723817C>A | CA373793316 | ROR2 | c.2677G>T (p.Gly893Cys) c.1920+337G>T (n.1920+337G>T) n.3145G>T c.2257G>T (p.Gly753Cys) c.1474G>T (p.Gly492Cys) c.2668G>T (p.Gly890Cys) | |
| 9 | g.91723817C= | CA1863921642 | ROR2 | c.2677G= (p.Gly893=) c.1920+337G= (n.1920+337G=) n.3145G= c.2257G= (p.Gly753=) c.1474G= (p.Gly492=) c.2668G= (p.Gly890=) | |
| 9 | g.91723817C>G | CA5120338 | ROR2 | c.2677G>C (p.Gly893Arg) c.1920+337G>C (n.1920+337G>C) n.3145G>C c.2257G>C (p.Gly753Arg) c.1474G>C (p.Gly492Arg) c.2668G>C (p.Gly890Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723817C>T | CA373793317 | ROR2 | c.2677G>A (p.Gly893Ser) c.1920+337G>A (n.1920+337G>A) n.3145G>A c.2257G>A (p.Gly753Ser) c.1474G>A (p.Gly492Ser) c.2668G>A (p.Gly890Ser) | dbSNP gnomAD v4 |
| 9 | g.91723818C>A | CA373793318 | ROR2 | c.2676G>T (p.Glu892Asp) c.1920+336G>T (n.1920+336G>T) n.3144G>T c.2256G>T (p.Glu752Asp) c.1473G>T (p.Glu491Asp) c.2667G>T (p.Glu889Asp) | |
| 9 | g.91723818C>G | CA373793319 | ROR2 | c.2676G>C (p.Glu892Asp) c.1920+336G>C (n.1920+336G>C) n.3144G>C c.2256G>C (p.Glu752Asp) c.1473G>C (p.Glu491Asp) c.2667G>C (p.Glu889Asp) | |
| 9 | g.91723818C>T | CA466334463 | ROR2 | c.2676G>A (p.Glu892=) c.1920+336G>A (n.1920+336G>A) n.3144G>A c.2256G>A (p.Glu752=) c.1473G>A (p.Glu491=) c.2667G>A (p.Glu889=) | gnomAD v4 |
| 9 | g.91723819T>A | CA373793322 | ROR2 | c.2675A>T (p.Glu892Val) c.1920+335A>T (n.1920+335A>T) n.3143A>T c.2255A>T (p.Glu752Val) c.1472A>T (p.Glu491Val) c.2666A>T (p.Glu889Val) | |
| 9 | g.91723819T>C | CA373793321 | ROR2 | c.2675A>G (p.Glu892Gly) c.1920+335A>G (n.1920+335A>G) n.3143A>G c.2255A>G (p.Glu752Gly) c.1472A>G (p.Glu491Gly) c.2666A>G (p.Glu889Gly) | gnomAD v4 |
| 9 | g.91723819T>G | CA373793320 | ROR2 | c.2675A>C (p.Glu892Ala) c.1920+335A>C (n.1920+335A>C) n.3143A>C c.2255A>C (p.Glu752Ala) c.1472A>C (p.Glu491Ala) c.2666A>C (p.Glu889Ala) | |
| 9 | g.91723820C>A | CA373793323 | ROR2 | c.2674G>T (p.Glu892Ter) c.1920+334G>T (n.1920+334G>T) n.3142G>T c.2254G>T (p.Glu752Ter) c.1471G>T (p.Glu491Ter) c.2665G>T (p.Glu889Ter) | |
| 9 | g.91723820C>G | CA373793324 | ROR2 | c.2674G>C (p.Glu892Gln) c.1920+334G>C (n.1920+334G>C) n.3142G>C c.2254G>C (p.Glu752Gln) c.1471G>C (p.Glu491Gln) c.2665G>C (p.Glu889Gln) | gnomAD v4 COSMIC |
| 9 | g.91723820C>T | CA373793325 | ROR2 | c.2674G>A (p.Glu892Lys) c.1920+334G>A (n.1920+334G>A) n.3142G>A c.2254G>A (p.Glu752Lys) c.1471G>A (p.Glu491Lys) c.2665G>A (p.Glu889Lys) | |
| 9 | g.91723821T>A | CA466334464 | ROR2 | c.2673A>T (p.Ser891=) c.1920+333A>T (n.1920+333A>T) n.3141A>T c.2253A>T (p.Ser751=) c.1470A>T (p.Ser490=) c.2664A>T (p.Ser888=) | |
| 9 | g.91723821T>C | CA466334465 | ROR2 | c.2673A>G (p.Ser891=) c.1920+333A>G (n.1920+333A>G) n.3141A>G c.2253A>G (p.Ser751=) c.1470A>G (p.Ser490=) c.2664A>G (p.Ser888=) | gnomAD v4 |
| 9 | g.91723821T>G | CA466334466 | ROR2 | c.2673A>C (p.Ser891=) c.1920+333A>C (n.1920+333A>C) n.3141A>C c.2253A>C (p.Ser751=) c.1470A>C (p.Ser490=) c.2664A>C (p.Ser888=) | gnomAD v4 |
| 9 | g.91723822G>A | CA373793326 | ROR2 | c.2672C>T (p.Ser891Leu) c.1920+332C>T (n.1920+332C>T) n.3140C>T c.2252C>T (p.Ser751Leu) c.1469C>T (p.Ser490Leu) c.2663C>T (p.Ser888Leu) | COSMIC |
| 9 | g.91723822G>C | CA373793327 | ROR2 | c.2672C>G (p.Ser891Ter) c.1920+332C>G (n.1920+332C>G) n.3140C>G c.2252C>G (p.Ser751Ter) c.1469C>G (p.Ser490Ter) c.2663C>G (p.Ser888Ter) | |
| 9 | g.91723822G>T | CA373793328 | ROR2 | c.2672C>A (p.Ser891Ter) c.1920+332C>A (n.1920+332C>A) n.3140C>A c.2252C>A (p.Ser751Ter) c.1469C>A (p.Ser490Ter) c.2663C>A (p.Ser888Ter) | |
| 9 | g.91723823A>C | CA373793329 | ROR2 | c.2671T>G (p.Ser891Ala) c.1920+331T>G (n.1920+331T>G) n.3139T>G c.2251T>G (p.Ser751Ala) c.1468T>G (p.Ser490Ala) c.2662T>G (p.Ser888Ala) | |
| 9 | g.91723823A>G | CA373793331 | ROR2 | c.2671T>C (p.Ser891Pro) c.1920+331T>C (n.1920+331T>C) n.3139T>C c.2251T>C (p.Ser751Pro) c.1468T>C (p.Ser490Pro) c.2662T>C (p.Ser888Pro) | |
| 9 | g.91723823A>T | CA373793330 | ROR2 | c.2671T>A (p.Ser891Thr) c.1920+331T>A (n.1920+331T>A) n.3139T>A c.2251T>A (p.Ser751Thr) c.1468T>A (p.Ser490Thr) c.2662T>A (p.Ser888Thr) | |
| 9 | g.91723824G>A | CA466334467 | ROR2 | c.2670C>T (p.Leu890=) c.1920+330C>T (n.1920+330C>T) n.3138C>T c.2250C>T (p.Leu750=) c.1467C>T (p.Leu489=) c.2661C>T (p.Leu887=) | |
| 9 | g.91723824G>C | CA466334468 | ROR2 | c.2670C>G (p.Leu890=) c.1920+330C>G (n.1920+330C>G) n.3138C>G c.2250C>G (p.Leu750=) c.1467C>G (p.Leu489=) c.2661C>G (p.Leu887=) | |
| 9 | g.91723824G>T | CA466334469 | ROR2 | c.2670C>A (p.Leu890=) c.1920+330C>A (n.1920+330C>A) n.3138C>A c.2250C>A (p.Leu750=) c.1467C>A (p.Leu489=) c.2661C>A (p.Leu887=) | |
| 9 | g.91723825A>C | CA373793332 | ROR2 | c.2669T>G (p.Leu890Arg) c.1920+329T>G (n.1920+329T>G) n.3137T>G c.2249T>G (p.Leu750Arg) c.1466T>G (p.Leu489Arg) c.2660T>G (p.Leu887Arg) | |
| 9 | g.91723825A>G | CA373793333 | ROR2 | c.2669T>C (p.Leu890Pro) c.1920+329T>C (n.1920+329T>C) n.3137T>C c.2249T>C (p.Leu750Pro) c.1466T>C (p.Leu489Pro) c.2660T>C (p.Leu887Pro) | |
| 9 | g.91723825A>T | CA373793334 | ROR2 | c.2669T>A (p.Leu890His) c.1920+329T>A (n.1920+329T>A) n.3137T>A c.2249T>A (p.Leu750His) c.1466T>A (p.Leu489His) c.2660T>A (p.Leu887His) | |
| 9 | g.91723826G>A | CA5120339 | ROR2 | c.2668C>T (p.Leu890Phe) c.1920+328C>T (n.1920+328C>T) n.3136C>T c.2248C>T (p.Leu750Phe) c.1465C>T (p.Leu489Phe) c.2659C>T (p.Leu887Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723826G>C | CA373793335 | ROR2 | c.2668C>G (p.Leu890Val) c.1920+328C>G (n.1920+328C>G) n.3136C>G c.2248C>G (p.Leu750Val) c.1465C>G (p.Leu489Val) c.2659C>G (p.Leu887Val) | |
| 9 | g.91723826G= | CA1863921643 | ROR2 | c.2668C= (p.Leu890=) c.1920+328C= (n.1920+328C=) n.3136C= c.2248C= (p.Leu750=) c.1465C= (p.Leu489=) c.2659C= (p.Leu887=) | |
| 9 | g.91723826G>T | CA373793336 | ROR2 | c.2668C>A (p.Leu890Ile) c.1920+328C>A (n.1920+328C>A) n.3136C>A c.2248C>A (p.Leu750Ile) c.1465C>A (p.Leu489Ile) c.2659C>A (p.Leu887Ile) | |
| 9 | g.91723827C>A | CA466334470 | ROR2 | c.2667G>T (p.Leu889=) c.1920+327G>T (n.1920+327G>T) n.3135G>T c.2247G>T (p.Leu749=) c.1464G>T (p.Leu488=) c.2658G>T (p.Leu886=) | |
| 9 | g.91723827C>G | CA466334471 | ROR2 | c.2667G>C (p.Leu889=) c.1920+327G>C (n.1920+327G>C) n.3135G>C c.2247G>C (p.Leu749=) c.1464G>C (p.Leu488=) c.2658G>C (p.Leu886=) | gnomAD v4 |
| 9 | g.91723827C>T | CA466334472 | ROR2 | c.2667G>A (p.Leu889=) c.1920+327G>A (n.1920+327G>A) n.3135G>A c.2247G>A (p.Leu749=) c.1464G>A (p.Leu488=) c.2658G>A (p.Leu886=) | |
| 9 | g.91723828A>C | CA373793337 | ROR2 | c.2666T>G (p.Leu889Arg) c.1920+326T>G (n.1920+326T>G) n.3134T>G c.2246T>G (p.Leu749Arg) c.1463T>G (p.Leu488Arg) c.2657T>G (p.Leu886Arg) | |
| 9 | g.91723828A>G | CA373793338 | ROR2 | c.2666T>C (p.Leu889Pro) c.1920+326T>C (n.1920+326T>C) n.3134T>C c.2246T>C (p.Leu749Pro) c.1463T>C (p.Leu488Pro) c.2657T>C (p.Leu886Pro) | gnomAD v4 |
| 9 | g.91723828A>T | CA373793339 | ROR2 | c.2666T>A (p.Leu889Gln) c.1920+326T>A (n.1920+326T>A) n.3134T>A c.2246T>A (p.Leu749Gln) c.1463T>A (p.Leu488Gln) c.2657T>A (p.Leu886Gln) | |
| 9 | g.91723829G>A | CA466334473 | ROR2 | c.2665C>T (p.Leu889=) c.1920+325C>T (n.1920+325C>T) n.3133C>T c.2245C>T (p.Leu749=) c.1462C>T (p.Leu488=) c.2656C>T (p.Leu886=) | |
| 9 | g.91723829G>C | CA373793340 | ROR2 | c.2665C>G (p.Leu889Val) c.1920+325C>G (n.1920+325C>G) n.3133C>G c.2245C>G (p.Leu749Val) c.1462C>G (p.Leu488Val) c.2656C>G (p.Leu886Val) | |
| 9 | g.91723829G>T | CA373793341 | ROR2 | c.2665C>A (p.Leu889Met) c.1920+325C>A (n.1920+325C>A) n.3133C>A c.2245C>A (p.Leu749Met) c.1462C>A (p.Leu488Met) c.2656C>A (p.Leu886Met) | gnomAD v4 |
| 9 | g.91723830G>A | CA466334476 | ROR2 | c.2664C>T (p.Ala888=) c.1920+324C>T (n.1920+324C>T) n.3132C>T c.2244C>T (p.Ala748=) c.1461C>T (p.Ala487=) c.2655C>T (p.Ala885=) | |
| 9 | g.91723830G>C | CA466334475 | ROR2 | c.2664C>G (p.Ala888=) c.1920+324C>G (n.1920+324C>G) n.3132C>G c.2244C>G (p.Ala748=) c.1461C>G (p.Ala487=) c.2655C>G (p.Ala885=) | |
| 9 | g.91723830G>T | CA466334474 | ROR2 | c.2664C>A (p.Ala888=) c.1920+324C>A (n.1920+324C>A) n.3132C>A c.2244C>A (p.Ala748=) c.1461C>A (p.Ala487=) c.2655C>A (p.Ala885=) | |
| 9 | g.91723831G>A | CA373793344 | ROR2 | c.2663C>T (p.Ala888Val) c.1920+323C>T (n.1920+323C>T) n.3131C>T c.2243C>T (p.Ala748Val) c.1460C>T (p.Ala487Val) c.2654C>T (p.Ala885Val) | |
| 9 | g.91723831G>C | CA373793342 | ROR2 | c.2663C>G (p.Ala888Gly) c.1920+323C>G (n.1920+323C>G) n.3131C>G c.2243C>G (p.Ala748Gly) c.1460C>G (p.Ala487Gly) c.2654C>G (p.Ala885Gly) | |
| 9 | g.91723831G>T | CA373793343 | ROR2 | c.2663C>A (p.Ala888Asp) c.1920+323C>A (n.1920+323C>A) n.3131C>A c.2243C>A (p.Ala748Asp) c.1460C>A (p.Ala487Asp) c.2654C>A (p.Ala885Asp) | gnomAD v4 |
| 9 | g.91723832C>A | CA373793345 | ROR2 | c.2662G>T (p.Ala888Ser) c.1920+322G>T (n.1920+322G>T) n.3130G>T c.2242G>T (p.Ala748Ser) c.1459G>T (p.Ala487Ser) c.2653G>T (p.Ala885Ser) | |
| 9 | g.91723832C>G | CA373793346 | ROR2 | c.2662G>C (p.Ala888Pro) c.1920+322G>C (n.1920+322G>C) n.3130G>C c.2242G>C (p.Ala748Pro) c.1459G>C (p.Ala487Pro) c.2653G>C (p.Ala885Pro) | |
| 9 | g.91723832C>T | CA373793347 | ROR2 | c.2662G>A (p.Ala888Thr) c.1920+322G>A (n.1920+322G>A) n.3130G>A c.2242G>A (p.Ala748Thr) c.1459G>A (p.Ala487Thr) c.2653G>A (p.Ala885Thr) | |
| 9 | g.91723833T>A | CA466334477 | ROR2 | c.2661A>T (p.Ala887=) c.1920+321A>T (n.1920+321A>T) n.3129A>T c.2241A>T (p.Ala747=) c.1458A>T (p.Ala486=) c.2652A>T (p.Ala884=) | |
| 9 | g.91723833T>C | CA466334478 | ROR2 | c.2661A>G (p.Ala887=) c.1920+321A>G (n.1920+321A>G) n.3129A>G c.2241A>G (p.Ala747=) c.1458A>G (p.Ala486=) c.2652A>G (p.Ala884=) | |
| 9 | g.91723833T>G | CA466334479 | ROR2 | c.2661A>C (p.Ala887=) c.1920+321A>C (n.1920+321A>C) n.3129A>C c.2241A>C (p.Ala747=) c.1458A>C (p.Ala486=) c.2652A>C (p.Ala884=) | |
| 9 | g.91723834G>A | CA373793348 | ROR2 | c.2660C>T (p.Ala887Val) c.1920+320C>T (n.1920+320C>T) n.3128C>T c.2240C>T (p.Ala747Val) c.1457C>T (p.Ala486Val) c.2651C>T (p.Ala884Val) | gnomAD v4 |
| 9 | g.91723834G>C | CA373793349 | ROR2 | c.2660C>G (p.Ala887Gly) c.1920+320C>G (n.1920+320C>G) n.3128C>G c.2240C>G (p.Ala747Gly) c.1457C>G (p.Ala486Gly) c.2651C>G (p.Ala884Gly) | |
| 9 | g.91723834G>T | CA373793350 | ROR2 | c.2660C>A (p.Ala887Glu) c.1920+320C>A (n.1920+320C>A) n.3128C>A c.2240C>A (p.Ala747Glu) c.1457C>A (p.Ala486Glu) c.2651C>A (p.Ala884Glu) | |
| 9 | g.91723835C>A | CA373793351 | ROR2 | c.2659G>T (p.Ala887Ser) c.1920+319G>T (n.1920+319G>T) n.3127G>T c.2239G>T (p.Ala747Ser) c.1456G>T (p.Ala486Ser) c.2650G>T (p.Ala884Ser) | |
| 9 | g.91723835C= | CA1863921644 | ROR2 | c.2659G= (p.Ala887=) c.1920+319G= (n.1920+319G=) n.3127G= c.2239G= (p.Ala747=) c.1456G= (p.Ala486=) c.2650G= (p.Ala884=) | |
| 9 | g.91723835C>G | CA373793352 | ROR2 | c.2659G>C (p.Ala887Pro) c.1920+319G>C (n.1920+319G>C) n.3127G>C c.2239G>C (p.Ala747Pro) c.1456G>C (p.Ala486Pro) c.2650G>C (p.Ala884Pro) | |
| 9 | g.91723835C>T | CA373793353 | ROR2 | c.2659G>A (p.Ala887Thr) c.1920+319G>A (n.1920+319G>A) n.3127G>A c.2239G>A (p.Ala747Thr) c.1456G>A (p.Ala486Thr) c.2650G>A (p.Ala884Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723836C>A | CA373793354 | ROR2 | c.2658G>T (p.Arg886Ser) c.1920+318G>T (n.1920+318G>T) n.3126G>T c.2238G>T (p.Arg746Ser) c.1455G>T (p.Arg485Ser) c.2649G>T (p.Arg883Ser) | |
| 9 | g.91723836C>G | CA373793355 | ROR2 | c.2658G>C (p.Arg886Ser) c.1920+318G>C (n.1920+318G>C) n.3126G>C c.2238G>C (p.Arg746Ser) c.1455G>C (p.Arg485Ser) c.2649G>C (p.Arg883Ser) | |
| 9 | g.91723836C>T | CA466334480 | ROR2 | c.2658G>A (p.Arg886=) c.1920+318G>A (n.1920+318G>A) n.3126G>A c.2238G>A (p.Arg746=) c.1455G>A (p.Arg485=) c.2649G>A (p.Arg883=) | |
| 9 | g.91723837C>A | CA373793356 | ROR2 | c.2657G>T (p.Arg886Met) c.1920+317G>T (n.1920+317G>T) n.3125G>T c.2237G>T (p.Arg746Met) c.1454G>T (p.Arg485Met) c.2648G>T (p.Arg883Met) | |
| 9 | g.91723837C>G | CA373793357 | ROR2 | c.2657G>C (p.Arg886Thr) c.1920+317G>C (n.1920+317G>C) n.3125G>C c.2237G>C (p.Arg746Thr) c.1454G>C (p.Arg485Thr) c.2648G>C (p.Arg883Thr) | gnomAD v4 |
| 9 | g.91723837C>T | CA373793358 | ROR2 | c.2657G>A (p.Arg886Lys) c.1920+317G>A (n.1920+317G>A) n.3125G>A c.2237G>A (p.Arg746Lys) c.1454G>A (p.Arg485Lys) c.2648G>A (p.Arg883Lys) | |
| 9 | g.91723838T>A | CA5120340 | ROR2 | c.2656A>T (p.Arg886Trp) c.1920+316A>T (n.1920+316A>T) n.3124A>T c.2236A>T (p.Arg746Trp) c.1453A>T (p.Arg485Trp) c.2647A>T (p.Arg883Trp) | dbSNP ExAC gnomAD v2 |
| 9 | g.91723838T>C | CA373793359 | ROR2 | c.2656A>G (p.Arg886Gly) c.1920+316A>G (n.1920+316A>G) n.3124A>G c.2236A>G (p.Arg746Gly) c.1453A>G (p.Arg485Gly) c.2647A>G (p.Arg883Gly) | dbSNP |
| 9 | g.91723838T>G | CA466334481 | ROR2 | c.2656A>C (p.Arg886=) c.1920+316A>C (n.1920+316A>C) n.3124A>C c.2236A>C (p.Arg746=) c.1453A>C (p.Arg485=) c.2647A>C (p.Arg883=) | |
| 9 | g.91723838T= | CA1863921647 | ROR2 | c.2656A= (p.Arg886=) c.1920+316A= (n.1920+316A=) n.3124A= c.2236A= (p.Arg746=) c.1453A= (p.Arg485=) c.2647A= (p.Arg883=) | |
| 9 | g.91723839G>A | CA466334482 | ROR2 | c.2655C>T (p.Asp885=) c.1920+315C>T (n.1920+315C>T) n.3123C>T c.2235C>T (p.Asp745=) c.1452C>T (p.Asp484=) c.2646C>T (p.Asp882=) | |
| 9 | g.91723839G>C | CA373793360 | ROR2 | c.2655C>G (p.Asp885Glu) c.1920+315C>G (n.1920+315C>G) n.3123C>G c.2235C>G (p.Asp745Glu) c.1452C>G (p.Asp484Glu) c.2646C>G (p.Asp882Glu) | |
| 9 | g.91723839G>T | CA373793361 | ROR2 | c.2655C>A (p.Asp885Glu) c.1920+315C>A (n.1920+315C>A) n.3123C>A c.2235C>A (p.Asp745Glu) c.1452C>A (p.Asp484Glu) c.2646C>A (p.Asp882Glu) | |
| 9 | g.91723840T>A | CA373793362 | ROR2 | c.2654A>T (p.Asp885Val) c.1920+314A>T (n.1920+314A>T) n.3122A>T c.2234A>T (p.Asp745Val) c.1451A>T (p.Asp484Val) c.2645A>T (p.Asp882Val) | |
| 9 | g.91723840T>C | CA373793363 | ROR2 | c.2654A>G (p.Asp885Gly) c.1920+314A>G (n.1920+314A>G) n.3122A>G c.2234A>G (p.Asp745Gly) c.1451A>G (p.Asp484Gly) c.2645A>G (p.Asp882Gly) | |
| 9 | g.91723840T>G | CA373793364 | ROR2 | c.2654A>C (p.Asp885Ala) c.1920+314A>C (n.1920+314A>C) n.3122A>C c.2234A>C (p.Asp745Ala) c.1451A>C (p.Asp484Ala) c.2645A>C (p.Asp882Ala) | |
| 9 | g.91723841C>A | CA373793367 | ROR2 | c.2653G>T (p.Asp885Tyr) c.1920+313G>T (n.1920+313G>T) n.3121G>T c.2233G>T (p.Asp745Tyr) c.1450G>T (p.Asp484Tyr) c.2644G>T (p.Asp882Tyr) | |
| 9 | g.91723841C= | CA1863921649 | ROR2 | c.2653G= (p.Asp885=) c.1920+313G= (n.1920+313G=) n.3121G= c.2233G= (p.Asp745=) c.1450G= (p.Asp484=) c.2644G= (p.Asp882=) | |
| 9 | g.91723841C>G | CA373793366 | ROR2 | c.2653G>C (p.Asp885His) c.1920+313G>C (n.1920+313G>C) n.3121G>C c.2233G>C (p.Asp745His) c.1450G>C (p.Asp484His) c.2644G>C (p.Asp882His) | |
| 9 | g.91723841C>T | CA373793365 | ROR2 | c.2653G>A (p.Asp885Asn) c.1920+313G>A (n.1920+313G>A) n.3121G>A c.2233G>A (p.Asp745Asn) c.1450G>A (p.Asp484Asn) c.2644G>A (p.Asp882Asn) | dbSNP gnomAD v4 |
| 9 | g.91723842T>A | CA466334483 | ROR2 | c.2652A>T (p.Ala884=) c.1920+312A>T (n.1920+312A>T) n.3120A>T c.2232A>T (p.Ala744=) c.1449A>T (p.Ala483=) c.2643A>T (p.Ala881=) | |
| 9 | g.91723842T>C | CA466334484 | ROR2 | c.2652A>G (p.Ala884=) c.1920+312A>G (n.1920+312A>G) n.3120A>G c.2232A>G (p.Ala744=) c.1449A>G (p.Ala483=) c.2643A>G (p.Ala881=) | |
| 9 | g.91723842T>G | CA466334485 | ROR2 | c.2652A>C (p.Ala884=) c.1920+312A>C (n.1920+312A>C) n.3120A>C c.2232A>C (p.Ala744=) c.1449A>C (p.Ala483=) c.2643A>C (p.Ala881=) | |
| 9 | g.91723843G>A | CA373793368 | ROR2 | c.2651C>T (p.Ala884Val) c.1920+311C>T (n.1920+311C>T) n.3119C>T c.2231C>T (p.Ala744Val) c.1448C>T (p.Ala483Val) c.2642C>T (p.Ala881Val) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723843G>C | CA373793369 | ROR2 | c.2651C>G (p.Ala884Gly) c.1920+311C>G (n.1920+311C>G) n.3119C>G c.2231C>G (p.Ala744Gly) c.1448C>G (p.Ala483Gly) c.2642C>G (p.Ala881Gly) | |
| 9 | g.91723843G= | CA1863921653 | ROR2 | c.2651C= (p.Ala884=) c.1920+311C= (n.1920+311C=) n.3119C= c.2231C= (p.Ala744=) c.1448C= (p.Ala483=) c.2642C= (p.Ala881=) | |
| 9 | g.91723843G>T | CA373793370 | ROR2 | c.2651C>A (p.Ala884Glu) c.1920+311C>A (n.1920+311C>A) n.3119C>A c.2231C>A (p.Ala744Glu) c.1448C>A (p.Ala483Glu) c.2642C>A (p.Ala881Glu) | |
| 9 | g.91723844C>A | CA373793371 | ROR2 | c.2650G>T (p.Ala884Ser) c.1920+310G>T (n.1920+310G>T) n.3118G>T c.2230G>T (p.Ala744Ser) c.1447G>T (p.Ala483Ser) c.2641G>T (p.Ala881Ser) | |
| 9 | g.91723844C= | CA1863921655 | ROR2 | c.2650G= (p.Ala884=) c.1920+310G= (n.1920+310G=) n.3118G= c.2230G= (p.Ala744=) c.1447G= (p.Ala483=) c.2641G= (p.Ala881=) | |
| 9 | g.91723844C>G | CA373793372 | ROR2 | c.2650G>C (p.Ala884Pro) c.1920+310G>C (n.1920+310G>C) n.3118G>C c.2230G>C (p.Ala744Pro) c.1447G>C (p.Ala483Pro) c.2641G>C (p.Ala881Pro) | |
| 9 | g.91723844C>T | CA373793373 | ROR2 | c.2650G>A (p.Ala884Thr) c.1920+310G>A (n.1920+310G>A) n.3118G>A c.2230G>A (p.Ala744Thr) c.1447G>A (p.Ala483Thr) c.2641G>A (p.Ala881Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723845C>A | CA373793374 | ROR2 | c.2649G>T (p.Met883Ile) c.1920+309G>T (n.1920+309G>T) n.3117G>T c.2229G>T (p.Met743Ile) c.1446G>T (p.Met482Ile) c.2640G>T (p.Met880Ile) | |
| 9 | g.91723845C= | CA1863921669 | ROR2 | c.2649G= (p.Met883=) c.1920+309G= (n.1920+309G=) n.3117G= c.2229G= (p.Met743=) c.1446G= (p.Met482=) c.2640G= (p.Met880=) | |
| 9 | g.91723845C>G | CA5120342 | ROR2 | c.2649G>C (p.Met883Ile) c.1920+309G>C (n.1920+309G>C) n.3117G>C c.2229G>C (p.Met743Ile) c.1446G>C (p.Met482Ile) c.2640G>C (p.Met880Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723845C>T | CA5120341 | ROR2 | c.2649G>A (p.Met883Ile) c.1920+309G>A (n.1920+309G>A) n.3117G>A c.2229G>A (p.Met743Ile) c.1446G>A (p.Met482Ile) c.2640G>A (p.Met880Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723846A= | CA1863921674 | ROR2 | c.2648T= (p.Met883=) c.1920+308T= (n.1920+308T=) n.3116T= c.2228T= (p.Met743=) c.1445T= (p.Met482=) c.2639T= (p.Met880=) | |
| 9 | g.91723846A>C | CA373793375 | ROR2 | c.2648T>G (p.Met883Arg) c.1920+308T>G (n.1920+308T>G) n.3116T>G c.2228T>G (p.Met743Arg) c.1445T>G (p.Met482Arg) c.2639T>G (p.Met880Arg) | |
| 9 | g.91723846A>G | CA5120343 | ROR2 | c.2648T>C (p.Met883Thr) c.1920+308T>C (n.1920+308T>C) n.3116T>C c.2228T>C (p.Met743Thr) c.1445T>C (p.Met482Thr) c.2639T>C (p.Met880Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723846A>T | CA373793376 | ROR2 | c.2648T>A (p.Met883Lys) c.1920+308T>A (n.1920+308T>A) n.3116T>A c.2228T>A (p.Met743Lys) c.1445T>A (p.Met482Lys) c.2639T>A (p.Met880Lys) | |
| 9 | g.91723847T>A | CA373793377 | ROR2 | c.2647A>T (p.Met883Leu) c.1920+307A>T (n.1920+307A>T) n.3115A>T c.2227A>T (p.Met743Leu) c.1444A>T (p.Met482Leu) c.2638A>T (p.Met880Leu) | |
| 9 | g.91723847T>C | CA373793378 | ROR2 | c.2647A>G (p.Met883Val) c.1920+307A>G (n.1920+307A>G) n.3115A>G c.2227A>G (p.Met743Val) c.1444A>G (p.Met482Val) c.2638A>G (p.Met880Val) | gnomAD v4 |
| 9 | g.91723847T>G | CA373793379 | ROR2 | c.2647A>C (p.Met883Leu) c.1920+307A>C (n.1920+307A>C) n.3115A>C c.2227A>C (p.Met743Leu) c.1444A>C (p.Met482Leu) c.2638A>C (p.Met880Leu) | |
| 9 | g.91723848G>A | CA466334487 | ROR2 | c.2646C>T (p.Ser882=) c.1920+306C>T (n.1920+306C>T) n.3114C>T c.2226C>T (p.Ser742=) c.1443C>T (p.Ser481=) c.2637C>T (p.Ser879=) | gnomAD v4 COSMIC |
| 9 | g.91723848G>C | CA466334488 | ROR2 | c.2646C>G (p.Ser882=) c.1920+306C>G (n.1920+306C>G) n.3114C>G c.2226C>G (p.Ser742=) c.1443C>G (p.Ser481=) c.2637C>G (p.Ser879=) | dbSNP |
| 9 | g.91723848G= | CA1863921680 | ROR2 | c.2646C= (p.Ser882=) c.1920+306C= (n.1920+306C=) n.3114C= c.2226C= (p.Ser742=) c.1443C= (p.Ser481=) c.2637C= (p.Ser879=) | |
| 9 | g.91723848G>T | CA466334486 | ROR2 | c.2646C>A (p.Ser882=) c.1920+306C>A (n.1920+306C>A) n.3114C>A c.2226C>A (p.Ser742=) c.1443C>A (p.Ser481=) c.2637C>A (p.Ser879=) | |
| 9 | g.91723849G>A | CA373793381 | ROR2 | c.2645C>T (p.Ser882Phe) c.1920+305C>T (n.1920+305C>T) n.3113C>T c.2225C>T (p.Ser742Phe) c.1442C>T (p.Ser481Phe) c.2636C>T (p.Ser879Phe) | gnomAD v4 COSMIC |
| 9 | g.91723849G>C | CA5120344 | ROR2 | c.2645C>G (p.Ser882Cys) c.1920+305C>G (n.1920+305C>G) n.3113C>G c.2225C>G (p.Ser742Cys) c.1442C>G (p.Ser481Cys) c.2636C>G (p.Ser879Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723849G= | CA1863921684 | ROR2 | c.2645C= (p.Ser882=) c.1920+305C= (n.1920+305C=) n.3113C= c.2225C= (p.Ser742=) c.1442C= (p.Ser481=) c.2636C= (p.Ser879=) | |
| 9 | g.91723849G>T | CA373793380 | ROR2 | c.2645C>A (p.Ser882Tyr) c.1920+305C>A (n.1920+305C>A) n.3113C>A c.2225C>A (p.Ser742Tyr) c.1442C>A (p.Ser481Tyr) c.2636C>A (p.Ser879Tyr) | gnomAD v4 |
| 9 | g.91723850A>C | CA373793382 | ROR2 | c.2644T>G (p.Ser882Ala) c.1920+304T>G (n.1920+304T>G) n.3112T>G c.2224T>G (p.Ser742Ala) c.1441T>G (p.Ser481Ala) c.2635T>G (p.Ser879Ala) | |
| 9 | g.91723850A>G | CA373793383 | ROR2 | c.2644T>C (p.Ser882Pro) c.1920+304T>C (n.1920+304T>C) n.3112T>C c.2224T>C (p.Ser742Pro) c.1441T>C (p.Ser481Pro) c.2635T>C (p.Ser879Pro) | |
| 9 | g.91723850A>T | CA373793384 | ROR2 | c.2644T>A (p.Ser882Thr) c.1920+304T>A (n.1920+304T>A) n.3112T>A c.2224T>A (p.Ser742Thr) c.1441T>A (p.Ser481Thr) c.2635T>A (p.Ser879Thr) | |
| 9 | g.91723851T>A | CA466334489 | ROR2 | c.2643A>T (p.Thr881=) c.1920+303A>T (n.1920+303A>T) n.3111A>T c.2223A>T (p.Thr741=) c.1440A>T (p.Thr480=) c.2634A>T (p.Thr878=) | |
| 9 | g.91723851T>C | CA466334490 | ROR2 | c.2643A>G (p.Thr881=) c.1920+303A>G (n.1920+303A>G) n.3111A>G c.2223A>G (p.Thr741=) c.1440A>G (p.Thr480=) c.2634A>G (p.Thr878=) | dbSNP |
| 9 | g.91723851T>G | CA466334491 | ROR2 | c.2643A>C (p.Thr881=) c.1920+303A>C (n.1920+303A>C) n.3111A>C c.2223A>C (p.Thr741=) c.1440A>C (p.Thr480=) c.2634A>C (p.Thr878=) | |
| 9 | g.91723852G>A | CA373793385 | ROR2 | c.2642C>T (p.Thr881Ile) c.1920+302C>T (n.1920+302C>T) n.3110C>T c.2222C>T (p.Thr741Ile) c.1439C>T (p.Thr480Ile) c.2633C>T (p.Thr878Ile) | gnomAD v4 |
| 9 | g.91723852G>C | CA373793386 | ROR2 | c.2642C>G (p.Thr881Arg) c.1920+302C>G (n.1920+302C>G) n.3110C>G c.2222C>G (p.Thr741Arg) c.1439C>G (p.Thr480Arg) c.2633C>G (p.Thr878Arg) | |
| 9 | g.91723852G>T | CA373793387 | ROR2 | c.2642C>A (p.Thr881Lys) c.1920+302C>A (n.1920+302C>A) n.3110C>A c.2222C>A (p.Thr741Lys) c.1439C>A (p.Thr480Lys) c.2633C>A (p.Thr878Lys) | |
| 9 | g.91723853T>A | CA373793388 | ROR2 | c.2641A>T (p.Thr881Ser) c.1920+301A>T (n.1920+301A>T) n.3109A>T c.2221A>T (p.Thr741Ser) c.1438A>T (p.Thr480Ser) c.2632A>T (p.Thr878Ser) | |
| 9 | g.91723853T>C | CA373793390 | ROR2 | c.2641A>G (p.Thr881Ala) c.1920+301A>G (n.1920+301A>G) n.3109A>G c.2221A>G (p.Thr741Ala) c.1438A>G (p.Thr480Ala) c.2632A>G (p.Thr878Ala) | |
| 9 | g.91723853T>G | CA373793389 | ROR2 | c.2641A>C (p.Thr881Pro) c.1920+301A>C (n.1920+301A>C) n.3109A>C c.2221A>C (p.Thr741Pro) c.1438A>C (p.Thr480Pro) c.2632A>C (p.Thr878Pro) | |
| 9 | g.91723854G>A | CA466334492 | ROR2 | c.2640C>T (p.Asn880=) c.1920+300C>T (n.1920+300C>T) n.3108C>T c.2220C>T (p.Asn740=) c.1437C>T (p.Asn479=) c.2631C>T (p.Asn877=) | |
| 9 | g.91723854G>C | CA373793391 | ROR2 | c.2640C>G (p.Asn880Lys) c.1920+300C>G (n.1920+300C>G) n.3108C>G c.2220C>G (p.Asn740Lys) c.1437C>G (p.Asn479Lys) c.2631C>G (p.Asn877Lys) | |
| 9 | g.91723854G>T | CA373793392 | ROR2 | c.2640C>A (p.Asn880Lys) c.1920+300C>A (n.1920+300C>A) n.3108C>A c.2220C>A (p.Asn740Lys) c.1437C>A (p.Asn479Lys) c.2631C>A (p.Asn877Lys) | |
| 9 | g.91723855T>A | CA373793393 | ROR2 | c.2639A>T (p.Asn880Ile) c.1920+299A>T (n.1920+299A>T) n.3107A>T c.2219A>T (p.Asn740Ile) c.1436A>T (p.Asn479Ile) c.2630A>T (p.Asn877Ile) | |
| 9 | g.91723855T>C | CA373793394 | ROR2 | c.2639A>G (p.Asn880Ser) c.1920+299A>G (n.1920+299A>G) n.3107A>G c.2219A>G (p.Asn740Ser) c.1436A>G (p.Asn479Ser) c.2630A>G (p.Asn877Ser) | gnomAD v4 |
| 9 | g.91723855T>G | CA373793395 | ROR2 | c.2639A>C (p.Asn880Thr) c.1920+299A>C (n.1920+299A>C) n.3107A>C c.2219A>C (p.Asn740Thr) c.1436A>C (p.Asn479Thr) c.2630A>C (p.Asn877Thr) | |
| 9 | g.91723856T>A | CA373793396 | ROR2 | c.2638A>T (p.Asn880Tyr) c.1920+298A>T (n.1920+298A>T) n.3106A>T c.2218A>T (p.Asn740Tyr) c.1435A>T (p.Asn479Tyr) c.2629A>T (p.Asn877Tyr) | |
| 9 | g.91723856T>C | CA373793397 | ROR2 | c.2638A>G (p.Asn880Asp) c.1920+298A>G (n.1920+298A>G) n.3106A>G c.2218A>G (p.Asn740Asp) c.1435A>G (p.Asn479Asp) c.2629A>G (p.Asn877Asp) | |
| 9 | g.91723856T>G | CA373793398 | ROR2 | c.2638A>C (p.Asn880His) c.1920+298A>C (n.1920+298A>C) n.3106A>C c.2218A>C (p.Asn740His) c.1435A>C (p.Asn479His) c.2629A>C (p.Asn877His) |